The document discusses the structures and properties of quinoline, isoquinoline, and indole. Quinoline and isoquinoline are fused aromatic ring systems consisting of benzene fused to pyridine with the nitrogen at different positions. Indole is a fused aromatic ring system consisting of benzene fused to pyrrole. The structures are described including hybridization and delocalized pi orbitals. Common preparation methods are outlined such as Skraup synthesis for quinoline and Bischler-Napieralski synthesis for isoquinoline. Key chemical reactions including electrophilic substitution, reduction, and reactions with acids and bases are also summarized.

1. Heterocyclic Chemistry
Fused ring systems
Mr. C. Naresh Babu
Assistant Professor
Email: nareshbabu.cvn@gmail.com

2. 2
Quinoline – Molecular Formula – C9H7N
• In quinoline all ring atoms (9 carbons and 1
nitrogen) are SP2 hybridized.
• Two SP2 orbitals on each atom overlap with each
other to form the C-C and C-N σ bonds. The third SP2
orbital on each carbon atom overlaps with an S orbital
of hydrogen and forms C-H σ bonds.
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP
Quinoline is a Fused aromatic ring system also known as benzo(b)pyridine.
•The third SP2 orbital of nitrogen is occupied by the nitrogen lone pair of
electrons.
• Each ring atom possess one un hybridized p – orbital containing one
electron and those are perpendicular to the plane containing the σ bonds.

3. • Overlap of these p – orbitals produces delocalized π – molecular
orbital containing 10 electrons.
• Quinoline shows aromatic properties because the resulting
molecular orbital satisfies the Huckle’s rule (4n+2 rule).
• The nitrogen lone pair is not released into the aromatic system
because it is perpendicular to the  system.
•The nitrogen withdraws electrons by resonance, resulting in an
electron-deficient ring system.
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 3

4. Preparations
1. Skraup Synthesis:
 Here a mixture of glycerol (propane- 1,2,3-triol), aniline
(phenylamine), sulfuric acid, nitrobenzene and ferrous [iron(II)]
sulfate are heated together.
 The reaction is exothermic and tends to become very violent.
 ferrous [iron(II)] sulfate is added to make the reaction less
violent.
 Nitrobenzene, or an alternative oxidant (iodine or chloroaniline
are often recommended), is required to convert the product, 1,2-
dihydroquinoline into quinoline.
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 4

5. Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 5
Skraup Synthesis

6. 2. Friedlander Synthesis: It involves condensation of o-amino
benzaldehyde with acetaldehyde in the presence of an alkali.
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 6
O
N H 2
o - a m i n o b e n z a l d e h y d e
C H 3 C H O
a c e t a l d e h y d e N
Q u i n o l i n e
- 2 H 2 O

7. Basic Character:
• Quinoline is slightly weaker base than pyridine. It reacts with acids
to yield salts which are sparingly soluble in water.
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 7
N
Quinoline
HCl
N
H
Cl
Quinoline
Hydrogen chloride

8. Chemical reactions:
1. Electrophilic substitution reactions: Takes at C5 & C8 positions.
a) Nitration:
b) Sulphonation
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 8
N
Q u i n o l i n e
H N O 3
N
H 2 S O 4
N
N O 2
N O 2
8 - n i t r o q u i n o l i n e
5 - n i t r o q u i n o l i n e
N
Q u i n o l i n e
N
H 2 S O 4
N
S O 3 H
S O 3 H
q u i n o l i n e - 8 - s u l f o n i c a c i d
q u i n o l i n e - 5 - s u l f o n i c a c i d

9. Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 9
2. Nucleophilic substitution reactions:
Reaction with sodamide: Substitution mostly happens at C-2 position, if any
substitution present at C-2 position then reaction occur at C-4 position.
3. Reaction with KOH:
4. Reaction with n-butyl lithium
N
Quinoline
N
NaNH2
Liq. NH3
NH2
quinolin-2-amine
N
Quinoline
N OH
KOH
quinolin-2-ol
N
Quinoline
N C
H2
C4H9Li
quinolin-2-ol
H2
C
C
H2
CH3- LiH

10. 10
5. Reaction with per acetic acid:
6. Reaction with KMnO4:
7. Reduction:
N
Quinoline
N
CH3
O
O
HO
peracetic acid
O
Quinoline-N-oxide
N
Q u i n o l i n e
N
K M n O 4
H O O C
H O O C
p y r i d i n e - 2 , 3 - d i c a r b o x y l i c a c i d
Q u i n o l i n i c a c i d
N
Q u i n o l i n e
N
H
N
H
1 , 2 , 3 , 4 - t e t r a h y d r o q u i n o l i n e
d e c a h y d r o q u i n o l i n e
S n / H C l
H 2 / P t
1 4 0 0
C

11. 11
8. Reaction with alkyl halides:
N
Q u i n o l i n e
N
C H 3 I
C H 3
I
N - m e t h y l q u i n o l i u m i o d i d e

12. 12
Isoquinoline – Molecular Formula – C9H7N
• In isoquinoline all ring atoms (9 carbons and 1
nitrogen) are SP2 hybridized.
• Two SP2 orbitals on each atom overlap with each
other to form the C-C and C-N σ bonds. The third SP2
orbital on each carbon atom overlaps with an S orbital
of hydrogen and forms C-H σ bonds.
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP
Isoquinoline is a Fused aromatic ring system also known as benzo(c)pyridine.
•The third SP2 orbital of nitrogen is occupied by the nitrogen lone pair of
electrons.
• Each ring atom possess one un hybridized p – orbital containing one
electron and those are perpendicular to the plane containing the σ bonds.

13. • Overlap of these p – orbitals produces delocalized π – molecular
orbital containing 10 electrons.
• Isoquinoline shows aromatic properties because the resulting
molecular orbital satisfies the Huckle’s rule (4n+2 rule).
• The nitrogen lone pair is not released into the aromatic system
because it is perpendicular to the  system.
•The nitrogen withdraws electrons by resonance, resulting in an
electron-deficient ring system.
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 13

14. Preparations
1. Bischler-Napieralski Synthesis:
 This method is very useful for the construction of 1-substituted
3,4- dihydroisoquinolines, which if necessary can be oxidized to
isoquinolines.
 β-phenylethylamine is reacted with an acyl chloride and a base to
give the corresponding amide (R1 = H) and then this is cyclized to
a 3,4-dihydroisoquinoline by treatment with either phosphorus
pentoxide or phosphorus oxychloride. Finally, aromatization is
accomplished by heating the 3,4-dihydroisoquinoline over
palladium on charcoal.
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 14

15. Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 15

16. 2. Pictet-Spengler Synthesis:
β-phenylethylamine react with an aldehyde, the reaction intermediate
is an imine which, provided the benzene ring contains electron
donating groups, often ring closes under very mild acidic conditions.
Indeed, cyclization can occur under physiological conditions, and in
Nature this is an important step in the biosynthesis of many
tetrahydroisoquinoline alkaloids. This tetrahydroisoquinoline can be
dehydrogenated by palladium to form 1-substituted isoquinoline.
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 16

17. Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 17
N H 2
2-phenylethanam ine
R C H O
N
C
R
H
H +
N
3,4-dihydro-1-substituted
isoquinoline
N
P d
1-substituted isoquinoline
RR

18. Basic Character:
• Isoquinoline is slightly weaker base, It reacts with acids to yield
salts which are sparingly soluble in water.
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 18
N
HCl
N
H
Cl
isoquinoline IsoquinolineHydrochloride

19. Chemical reactions:
1. Electrophilic substitution reactions: It takes place at the
position 5.
a) Nitration:
b) Sulphonation
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 19
N
H N O 3
N
N O 2
i s o q u i n o l i n e
5 - n i t r o i s o q u i n o l i n e
N N
H2SO4
SO3H
isoquinoline isoquinoline-5-sulfonic acid

20. Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 20
c. Bromination:
2. Reduction:
N N
B r
i s o q u i n o l i n e
B r 2
5 - b r o m o i s o q u i n o l i n e
N
i s o q u i n o l i n e
N a - H g
S n c l 2
P t
H 2
H 2
H 2
N H N H
N H
1 , 2 - d i h y d r o i s o q u i n o l i n e 1 , 2 , 3 , 4 - t e t r a h y d r o i s o q u i n o l i n e
d e c a h y d r o i s o q u i n o l i n e

21. 21
3. Oxidation / Reaction with KMnO4:
4. Reaction with alkyl halide:
5. Reaction with sodamide:
N
N
K M n O 4
( O )
C O O H
C O O H
p y r i d i n e - 3 , 4 - d i c a r b o x y l i c a c i di s o q u i n o l i n e
C O O H
C O O H
p h t h a l i c a c i d
N N
C H 3 I
C H 3
C l
i s o q u i n o l i n e I s o q u i n a l o n i u m m e t h y l i o d i d e
N N
N a N H 2
i s o q u i n o l i n e
N H 2
i s o q u i n o l i n - 1 - a m i n e

22. 22
Indole – Molecular Formula – C8H7N
• In indole all ring atoms (8 carbons and 1
nitrogen) are SP2 hybridized.
• Two SP2 orbitals on each atom overlap with each
other to form the C-C and C-N σ bonds. The third SP2
orbital on each ring atom overlaps with an S orbital of
hydrogen and forms C-H and N-H σ bonds.
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP
Indole is a Fused aromatic ring system also known as benzo(b)pyrrole.
•The un hybridized p – orbital of nitrogen is occupied by the nitrogen
lone pair of electrons.
• Each carbon atom in ring possess one un hybridized p – orbital
containing one electron and those are perpendicular to the plane
containing the σ bonds.

23. • Overlap of these p – orbitals produces delocalized π – molecular
orbital containing 10 electrons. (8 electrons from 8 carbons and
lone pair of electrons from nitrogen)
• Indole shows aromatic properties because the resulting molecular
orbital satisfies the Huckle’s rule (4n+2 rule).
• The nitrogen lone pair is released into the aromatic system.
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 23

24. Preparations
1. Lipp Synthesis:
 In this method o-amino chlorostyrene is heated with sodium
ethoxide at 160-1700C.
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 24
N H 2
o - a m i n o c h l o r o s t y r e n e
H
C
C
H
C l
N a O C 2 H 5
N
H
I n d o l e
C 2 H 5 O H N a c l

25. Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 25
NH
NH2
Phenyl hydrazine
O
H3C O
OH
Pyruvic acid
N
H
-H2O
N
H3C COOH
ZnCl2
-NH3
N
H
COOH
Decarboxylation
N
H
1H-indole
-CO2
2. Fisher indole synthesis:
 Pyruvic acid is first treated wit phenyl hydrazine to form the corresponding phenyl
hydrazine.
 Then the hydrazine is heated with anhydrous zinc chloride or poly phosphoric acid
to give indole-2-carboxylic acid, which upon decarboxylation yields indole.

26. Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 26
3. Madelung synthesis:
 O-toluidine is react with formic acid to form N-formyl o-toluidine. This undergoes
dehydration on heating with sodium ethoxide or potassium t-butoxide to tield
indole.
C H 3
N H 2
o-toluidine
O
H O
H
form ic acid
- H 2O
C H 3
N
H
H
O
C2H 5O N a
C4H 9O -
K +
- H 2O
N
H
1H -indole

27. Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 27
4. From o-nitro phenyl acetaldehyde:
 This involves reduction of o-nitro phenyl acetaldehyde with iron powder and
sodium bisulphite to give o-amino phenyl acetaldehyde, which cyclizes
spontaneously to yield indole.
o-nitro phenyl acetaldehyde
Na+
O-
S
O
HO
Sodium bisulphite
O
NH2
o-amino phenylacetaldehyde
O
NO2
- H2O
N
H
1H-indole

28. Basic Character & Acidic character:
• Indole is a weak base and also a weak acid as like pyrrole.
• Indole is a weak base since the lone pair of electrons of nitrogen
atom contributes to the 4n+2 π electron cloud (aromatic sextet).
Thus, the availability of these lone pair of electrons is decreased.
• Indole also exhibit weak acidic properties, the weak acidic property
is because of its formation of potassium indole with KOH.
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 28
N
H
1 H - i n d o l e
K O H
N
K
- H 2 O
P o t a s s i u m i n d o l e

29. Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 29
Chemical reactions:
Electrophilic Substitution reactions (C-3 versus C-2):
 Electrophiles attack indole at C-3, rather than at C-2.
 This is the opposite result to that observed for pyrroles, but can be explained if the
intermediates for each type of reaction are considered.
 For a reaction at C-3, the energy of activation of the intermediate is lowered because
it is possible to delocalize the positive charge through resonance involving the
nitrogen lone pair of electrons.
 This favourable situation is not possible in the corresponding intermediate for attack
at C-2. Any attempt to delocalize the positive charge would now disrupt the 6π
electrons system of the benzene ring.

30. a) Nitration:
b) Sulphonation
c) Halogenation
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 30
N
H
1 H -in d o le
C 2 H 5 N O 2
E th y l n itra te
C 2 H 5 O N a
5 o
C
N
H
N O 2
3 -n itro -1 H -in d o le
N
H
1 H - i n d o l e
S O 3
P y r id i n e
1 1 0 o
C
N
H
S O 3 H
1 H - in d o l e - 3 - s u l f o n ic a c i d
N
H
1 H - in d o le
S O 2 C l2
B r - C H 3 O H
N
H
X
3 - h a lo 1 H - in d o le

31. d) Friedal-craft acylation
e) Formylation
f) Vilsmeyer reaction
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 31
N
H
1H -indole
C H 3C O C l
A cetyl chloride
S nC l4
N
H
C O C H 3
3-acetyl indole
N
H
1 H - in d o le
H C N - H C l
N
H
C H O
3 - f o rm y l- 1 H -in d o le
N
H
1 H - i n d o l e
N
H
C H O
3 - f o r m y l - 1 H - i n d o l e
N O
N - f o r m y l d i m e t h y l a m i n e
P O C l 3

32. g) Reimer – tiemann reaction:
h) Alkylation
i) Mannich reaction:
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 32
N
H
1 H - i n d o l e
C H C l 3
C h l o r o f o r m
N a O H
N
H
C H O
3 - f o r m y l i n d o l e
N
H
1 H - i n d o l e
D M F
N
H
C H 3
C H 3 I
3 - m e t h y l - 1 H - i n d o l e
N
H
1 H -in d o le
N
H
C H 2 -N (C H 3 )2
H C H O
H
N
C H 3H 3 C
D im e th y l a m in e
- H 2 O
3 -D im e th y l a m in o m e th y l-1 H -in d o le

33. j) Reduction: Mild reduction by Zn & HCl.
But catalyst Ni / Pt reduces both rings and forms octa hydro indole.
k) Diazo coupling:
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 33
N
H
1 H - i n d o l e
N
H
i n d o l i n e o r
2 , 3 - d i h y d r o - 1 H - i n d o l e
Z n / H C l
N
H
1 H - i n d o l e
N
H
N i / P t
o c t a h y d r o - 1 H - i n d o l e
N
H
1 H -in d o le
N +
N
C l-
B en zen e d iazo n iu m ch lo rid e N
H
NN
1 -(1 H -in d o l-3 -y l)-2 -p h en y ld iazen e

34. 34
Acridine – Molecular Formula – C13H9N
• In acridine all ring atoms (13 carbons and 1
nitrogen) are SP2 hybridized.
• Two SP2 orbitals on each atom overlap with each
other to form the C-C and C-N σ bonds. The third SP2
orbital on each carbon atom overlaps with an S orbital
of hydrogen and forms C-H σ bonds.
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP
Acridine is a Fused aromatic ring system also known as Dibenzo[b,e]pyridine
/ 2,3-Benzoquinoline
•The third SP2 orbital of nitrogen is occupied by the lone pair of electron
of nitrogen.
• Each ring atom in ring possess one un hybridized p – orbital containing
one electron and those are perpendicular to the plane containing the σ
bonds.

35. • Overlap of these p – orbitals produces delocalized π – molecular
orbital containing 14 electrons.
• Acridine shows aromatic properties because the resulting
molecular orbital satisfies the Huckle’s rule (4n+2 rule).
• The nitrogen lone pair is not released into the aromatic system.
• It is a planar molecule that is structurally related to anthracene with
one of the central CH group is replaced by nitrogen.
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 35

36. Preparations
1. From diphenyl amine-2-carboxylic acid:
36
O
HO
Cl
o-chloro benzoic acid
H2N
Aniline
Base
N
H
COOH
Diphenylamine-2-carboxylic acid
H2SO4
POCl3
N
H
O
N
H
Cl
9-chloro-9,10-dihydroacridine
acridin-9(10H)-one
Na / Amyl
alcohol
H2 / Ni
N
H
9,10-dihydroacridine
Oxidation
N
Acridine

37. Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 37
2. From o-amino diphenyl methane:
Acridine is also prepared by passing o-amino diphenyl methane
through a red hot tube.
Basic character:
Acridine is a weak base but it forms soluble salts with mineral acids.
N H 2
o - a m i n o d i p h e n y l m e t h a n e
R e d h o t t u b e
N
A c r i d i n e
N
A c r i d i n e
H C l
N
H
C l
A c r i d i n e h y d r o c h l o r i d e

38. Chemical reactions:
1. Electrophilic substitution reactions:
Halogenation:
2. Reaction with nucleophilic reagents
 Acridine easily reacted with nucleophilic reagents.
 Nucleophilic attack takes place at 9-position, because the electron
density is decreased at this position when compare to 1,2,3 and 4th
positions.
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 38
N
A cridine
B r2
C H 3C O O H
N
N
B r
B rB r
2,7-dibrom oacridine
2-brom oacridine

39. Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 39
 So, Acridine easily reacted with sodamide in liq. Ammonia, it gives 9-
amino acridine.
3. Reaction with oxidizing agents:
N
A cridine
N aN H 2
L iq. N H 3
N
N H 2
9-A m ino acridine
N
A cridine
K M nO 4
N
N
C O O H
C O O H
quinoline-2,3-dicarboxylic acid
C H 3
O
O
H O
Peracetic acid
O A cridine-N -oxide
Acridine is very stable ring
system towards oxidizing
agents. But in the presence
of per acids acridine easily
converted to N-oxide.

40. Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 40
4. Reaction with reducing agents:
5. Reaction with alkyl halides:
Acridine readily reacts with alkyl halides for example with methyl iodide it gives N-
methyl acridinium iodide.
N
A c r i d i n e
H 2 / N i
N
H
9 , 1 0 - d i h y d r o a c r i d i n e
N
Acridine
CH3I
N
H3C
I
10-methyl Acridinium iodide

41. 41
Benzimidazole – Molecular Formula – C7H6N2
• In Benzimidazole all ring atoms (7 carbons and 2
nitrogens) are SP2 hybridized.
• Two SP2 orbitals on each atom overlap with each
other to form the C-C and C-N σ bonds.
•The third SP2 orbital on each carbon atom and one
nitrogen atom overlaps with an S orbital of hydrogen
and forms C-H and N-H σ bonds.
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP
Benzimidazole is a Fused aromatic ring system fusion of benzene and imidazole.
•The third SP2 orbital of second nitrogen is occupied by the lone pair of
electrons.
• Each carbon atom in ring possess one un hybridized p – orbital
containing one electron and those are perpendicular to the plane
containing the σ bonds.
Benzo(d)imidazole

42. • One of the nitrogen in benzimidazole having lone pair of electrons
are released into the aromatic system.
• Overlap of these p – orbitals, lone pair of electrons from one
nitrogen produces delocalized π – molecular orbital containing 10
electrons.
• Benzimidazole shows aromatic properties because the resulting
molecular orbital satisfies the Huckle’s rule (4n+2 rule).
• benzimidazoles display annular tautomerism in solution, e.g.
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 42

43. Preparations
1. From o-phenylenediamine / Phillips reaction:
It is the most important method of preparing benzimidazole by refluxing o-
phenylenediamine with a carboxylic acidnin 4N HCl.
43
NH2
NH2
o-phenylene diamine
OH
O
R
4N HCl, Reflux
N
N
H
2-Substituted Benzimidazole
R
- 2 H2O

44. Basic Character & Acidic character:
• Benzimidazole is a weak base and also a weak acid.
• Benzimidazole is a weak base because due to the presence of
lone pair of electrons on one of the nitrogen atom.
• Benzimidazole also exhibit weak acidic properties, the weak acidic
property is because of its formation of potassium phenothiazine
with KOH.
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 44
N
N
H
Benzimidazole
H Cl
N
N
H
H
Cl
Benzim idazole hydrochloride
N
N
H
K O H
- H 2O
N
N
K1H -benzo[d]im idazole
N -potassium benzimidazole

45. Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 45
Chemical reactions:
Electrophilic Substitution reactions:
 Electrophiles attack in benzimidazole take place preferentially at the 5- or 6-
position. However, the electrophile may also enter the 4- or 7-position if the 5- or 6-
position is blocked.
Nitration:
Sulphonation:
N
N
H
B e n z i m i d a z o l e
H N O 3
N
N
H
O 2 N
5 - n i t r o - 1 H - b e n z o [ d ] i m i d a z o l e
N
N
H
B e n z i m i d a z o l e
H 2 S O 4
N
N
H
H O 3 S
1 H - b e n z o [ d ] i m i d a z o l e - 5 - s u l f o n i c a c i d

46. Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 46
By treatment with acid anhydrides: 1-benzimidazoylmagnesium bromide when treated
with benzoyl chloride in ether solution gives mostly N,N’- dibenzoylbenzimidazole and
the rupture of the imidazole ring has been postulated by hydrolysis.

47. Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 47
Halogenation: When 2,5 (or 2,6)-dimethylbenzimidazole in an aqueous acid solution is
treated with a saturated solution of bleaching powder at 0 to 5°C, 1-chloro-2,5(or 2,6)-
dimethylbenzimidazole is obtained.
Nucleophilic substitution reaction:
Reaction with sodamide:
N
N
H
B e n z i m i d a z o l e
N a N H 2
N
N
H
N H 2
1 H - b e n z o [ d ] i m i d a z o l - 2 - a m i n e

48. Reduction: Mild reduction by Zn & HCl.
But catalyst Ni / Pt reduces both rings and forms octa hydro indole.
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 48
N
H
N
N
H
H
N
Z n / H C l
1 H - b e n z o [ d ] i m i d a z o l e 2 ,3 - d i h y d r o - 1 H - b e n z o [ d ] i m i d a z o l e
N
H
N
N
H
H
N
N i / P t
1 H - b e n z o [ d ] i m i d a z o l e o c t a h y d r o - 1 H - b e n z o [ d ] i m i d a z o l e

49. 49
Phenothiazine – Molecular Formula – C12H9NS
• In phenothiazine all ring atoms (12 carbons and
1 nitrogen and 1 sulphur) are SP2 hybridized.
• Two SP2 orbitals on each atom overlap with each
other to form the C-C and C-N and C-S σ bonds.
•The third SP2 orbital on each carbon atom and
nitrogen atom overlaps with an S orbital of hydrogen
and forms C-H and N-H σ bonds.
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP
Phenothiazine is a Fused aromatic ring system also known as Dibenzothiazine
•The third SP2 orbital of sulphur is occupied by the lone pair of electrons.
• Each carbon atom in ring possess one un hybridized p – orbital
containing one electron and those are perpendicular to the plane
containing the σ bonds.

50. • Overlap of these p – orbitals, lone pair of electrons from Sulphur
and nitrogen produces delocalized π – molecular orbital containing
14 electrons.
• Phenothiazine shows aromatic properties because the resulting
molecular orbital satisfies the Huckle’s rule (4n+2 rule).
• The nitrogen and Sulphur lone pair are released into the aromatic
system.
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 50

51. Preparations
1. From diphenyl amine:
It is prepared by fusing diphenyl amine with Sulphur.
2. From o-amino thiophenol:
It is prepared by heating o-amino thiophenol with catechol.
51
N
H
D i p h e n y l a m i n e
2 S
- H 2 S
S
N
H
P h e n o t h i a z i n e
N H 2
S H
o - a m i n o t h i o p h e n o l
H O
H O
C a t e c h o l
- 2 H 2 O
S
N
H
P h e n o t h i a z i n e

52. Basic Character & Acidic character:
Phenothiazine is a weak base and also a weak acid.
• Phenothiazine is a weak base since the lone pair of electrons of
nitrogen atom contributes to the 4n+2 π electron cloud. Thus, the
availability of these lone pair of electrons is decreased.
• Indole also exhibit weak acidic properties, the weak acidic property
is because of its formation of potassium phenothiazine with KOH.
Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 52
S
N
H
P h e n o t h i a z i n e
K O H
- H 2 O
S
N
K
P o t a s s i u m p h e n o t h i a z i n e

53. Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 53
1. Electrophilic substitution reactions:
Mostly the electrophilic substitution reactions happens at 2, 3, 7 and 8 th
positions.
S
H
N
Phenothiazine
Nitration
Sulphonation
Halogenation
S
H
N
S
H
N
S
H
N
NO2O2N HO3S SO3H
ClCl
Cl Cl
2,8-dinitro-10H-phenothiazine 10H-phenothiazine-2,8-disulfonic acid
2,3,7,8-tetrachloro-10H-phenothiazine

54. Mr. C. Naresh Babu, Asst. Professor, RIPER, ATP 54
2. Reaction of phenothiazine and n-butyl lithium followed by the addition
of solid carbon dioxide to the mixture and gives 1-carboxy phenothiazine.
3. Nucleophilic substitution reactions:
Mostly happens at 1 or 9th positions.
Reaction with sodamide:
S
H
N
P h e n o th ia z in e
N a N H 2
S
H
N
N H 2
1 0 H -p h e n o th ia z in -1 -a m in e