Product Name

  • Name

    PYRIDINE-2-SULFONYL CHLORIDE

  • EINECS
  • CAS No. 66715-65-9
  • Article Data61
  • CAS DataBase
  • Density 1.489 g/cm3
  • Solubility
  • Melting Point
  • Formula C5H4ClNO2S
  • Boiling Point 284.162 °C at 760 mmHg
  • Molecular Weight 177.611
  • Flash Point 125.657 °C
  • Transport Information
  • Appearance
  • Safety
  • Risk Codes
  • Molecular Structure Molecular Structure of 66715-65-9 (PYRIDINE-2-SULFONYL CHLORIDE)
  • Hazard Symbols
  • Synonyms 2-Pyridinylsulfonylchloride;2-Pyridylsulfonyl chloride;Pyridin-2-sulfonyl chloride;
  • PSA 55.41000
  • LogP 2.08990

Synthetic route

2-Mercaptopyridine
2637-34-5

2-Mercaptopyridine

pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

Conditions
ConditionsYield
With hydrogenchloride; chlorine at 5℃; for 0.5h;97%
With Oxone; potassium chloride In water at 20℃; for 0.166667h;88%
With hydrogenchloride; water; chlorine at 0℃; for 2h; Inert atmosphere;85%
2,2'-dipyridyldisulphide
2127-03-9

2,2'-dipyridyldisulphide

A

2-chloropyridine
109-09-1

2-chloropyridine

B

pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

Conditions
ConditionsYield
With 1,3-dichloro-5,5-dimethylhydantoin; acetic acid In dichloromethane; water at 0 - 20℃; Inert atmosphere;A 20%
B 78%
2-Mercaptopyridine
2637-34-5

2-Mercaptopyridine

chloroamine-T
127-65-1

chloroamine-T

A

pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

B

N-chloro-N-(4-methylbenzenesulfonyl)-pyridine-2-sulfinamide

N-chloro-N-(4-methylbenzenesulfonyl)-pyridine-2-sulfinamide

Conditions
ConditionsYield
With N-chloro-succinimide In water; acetonitrile at 35℃; for 0.25h;A 11%
B 57%
2-Mercaptopyridine
2637-34-5

2-Mercaptopyridine

hydrogenchloride
7647-01-0

hydrogenchloride

chlorine
7782-50-5

chlorine

pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

2-bromo-pyridine
109-04-6

2-bromo-pyridine

pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

Conditions
ConditionsYield
Stage #1: 2-bromo-pyridine With isopropylmagnesium chloride In tetrahydrofuran at 20℃; for 0.5h;
Stage #2: With sulfur dioxide In tetrahydrofuran at -40℃; for 0.5h;
Stage #3: With sulfuryl dichloride In tetrahydrofuran at -40 - 20℃;
Stage #1: 2-bromo-pyridine With n-butyllithium; dibutylmagnesium In tetrahydrofuran at -10℃; Inert atmosphere;
Stage #2: With sulfuryl dichloride In tetrahydrofuran; toluene at -10 - 10℃;
2-Mercaptopyridine
2637-34-5

2-Mercaptopyridine

sodium thiosulfate

sodium thiosulfate

pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

Conditions
ConditionsYield
In hydrogenchloride
2-Mercaptopyridine
2637-34-5

2-Mercaptopyridine

aq NaOCl

aq NaOCl

pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

Conditions
ConditionsYield
With conc HCl In dichloromethane; water
2-Mercaptopyridine
2637-34-5

2-Mercaptopyridine

aqueous sodium hypochlorite

aqueous sodium hypochlorite

pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

Conditions
ConditionsYield
With sulfuric acid; chlorine
2,2'-dipyridyldisulphide
2127-03-9

2,2'-dipyridyldisulphide

pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

Conditions
ConditionsYield
With hydrogenchloride; chlorine at -10 - -8℃; for 0.5h;
With hydrogenchloride; chlorine In water at -10℃; for 0.5h;
2-pyridinesulfinic acid sodium salt
24367-66-6

2-pyridinesulfinic acid sodium salt

pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

Conditions
ConditionsYield
With N-chloro-succinimide In dichloromethane
2-pyridinesulfonyl chloride hydrochloride
111480-84-3

2-pyridinesulfonyl chloride hydrochloride

pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

Conditions
ConditionsYield
In dichloromethane
pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

2-Benzyloxyethanol
622-08-2

2-Benzyloxyethanol

Pyridine-2-sulfonic acid 2-benzyloxy-ethyl ester
123455-81-2

Pyridine-2-sulfonic acid 2-benzyloxy-ethyl ester

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0℃;99%
pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

((3aR,4R,6R,6aR)-6-methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methanol
4099-85-8

((3aR,4R,6R,6aR)-6-methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methanol

Pyridine-2-sulfonic acid (3aR,4R,6R,6aR)-6-methoxy-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl ester
123455-86-7

Pyridine-2-sulfonic acid (3aR,4R,6R,6aR)-6-methoxy-2,2-dimethyl-tetrahydro-furo[3,4-d][1,3]dioxol-4-ylmethyl ester

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0℃;99%
pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

octanol
111-87-5

octanol

1-(2-Pyridylsulfonyl)oxo-octane

1-(2-Pyridylsulfonyl)oxo-octane

Conditions
ConditionsYield
With triethylamine In water; ethyl acetate99%
pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

C16H13NO
893733-67-0

C16H13NO

C21H16N2O3S
1443501-77-6

C21H16N2O3S

Conditions
ConditionsYield
Stage #1: C16H13NO With sodium hydride In tetrahydrofuran at 0℃;
Stage #2: pyridine-2-sulfonyl chloride In tetrahydrofuran at 0 - 20℃;
99%
piperidine
110-89-4

piperidine

pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

Piperidin-1-yl pyridin-2-yl sulfone
106762-43-0

Piperidin-1-yl pyridin-2-yl sulfone

Conditions
ConditionsYield
With potassium carbonate In diethyl ether at 0℃; for 3.5h;98%
In dichloromethane at 25℃; for 12h; Inert atmosphere;98%
In dichloromethane at 0 - 25℃; for 12h; Inert atmosphere;81%
In dichloromethane at 20℃; Cooling with ice;
pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

3-bromopropylamine hydrochloride
5003-71-4

3-bromopropylamine hydrochloride

N-(3-bromopropyl)-pyridine-2-sulfonamide
171825-88-0

N-(3-bromopropyl)-pyridine-2-sulfonamide

Conditions
ConditionsYield
With potassium carbonate In dichloromethane; water at 0℃; for 1h;98%
pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

diallylamine
124-02-7

diallylamine

N,N-Diallylpyridine-2-sulfonamide

N,N-Diallylpyridine-2-sulfonamide

Conditions
ConditionsYield
With potassium carbonate In diethyl ether at 0℃; for 1.5h;98%
pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

benzylamine
100-46-9

benzylamine

pyridine-2-sulfonic acid benzylamide
370839-64-8

pyridine-2-sulfonic acid benzylamide

Conditions
ConditionsYield
With triethylamine In dichloromethane98%
86%
pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

L-valine methylester hydrochloride
6306-52-1

L-valine methylester hydrochloride

(S)-mehyl 3-mehyl-2-(pyridine-2-sulfonamido)butanoate
1384331-68-3

(S)-mehyl 3-mehyl-2-(pyridine-2-sulfonamido)butanoate

Conditions
ConditionsYield
With N,N,N,N,-tetramethylethylenediamine In acetonitrile at 20℃; for 16h;98%
With pyridine In acetonitrile at 0 - 20℃; for 18h; Inert atmosphere; Sealed tube;98%
With triethylamine In dichloromethane at 0 - 20℃;117 mg
pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

non-1-yn-3-ol
7383-20-2

non-1-yn-3-ol

Pyridine-2-sulfonic acid 1-ethynyl-heptyl ester
123455-80-1

Pyridine-2-sulfonic acid 1-ethynyl-heptyl ester

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0℃;97%
pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

1,2:3,4-di-O-isopropylidene-α-D-galactopyranose
4064-06-6

1,2:3,4-di-O-isopropylidene-α-D-galactopyranose

Pyridine-2-sulfonic acid (3aR,5R,5aS,8aS,8bR)-2,2,7,7-tetramethyl-tetrahydro-bis[1,3]dioxolo[4,5-b;4',5'-d]pyran-5-ylmethyl ester
123455-87-8

Pyridine-2-sulfonic acid (3aR,5R,5aS,8aS,8bR)-2,2,7,7-tetramethyl-tetrahydro-bis[1,3]dioxolo[4,5-b;4',5'-d]pyran-5-ylmethyl ester

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0℃;97%
pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

L-phenylalanine tert-butyl ester
16874-17-2

L-phenylalanine tert-butyl ester

tert-Butyl 2-benzyl-2-<(pyridine-2-sulfonyl)amino>acetate

tert-Butyl 2-benzyl-2-<(pyridine-2-sulfonyl)amino>acetate

Conditions
ConditionsYield
With potassium carbonate In diethyl ether at 0℃; for 6h;97%
pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

6-isopropyl-1H-indole-3-carbaldehyde

6-isopropyl-1H-indole-3-carbaldehyde

C17H16N2O3S
1443501-79-8

C17H16N2O3S

Conditions
ConditionsYield
Stage #1: 6-isopropyl-1H-indole-3-carbaldehyde With sodium hydride In tetrahydrofuran at 0℃;
Stage #2: pyridine-2-sulfonyl chloride In tetrahydrofuran at 0 - 20℃;
97%
pyrrolidine
123-75-1

pyrrolidine

pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

2-(pyrrolidin-1-ylsulfonyl)pyridine
106762-45-2

2-(pyrrolidin-1-ylsulfonyl)pyridine

Conditions
ConditionsYield
In dichloromethane at 0 - 25℃; for 12h; Inert atmosphere;97%
In dichloromethane at 20℃; Cooling with ice;
pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

ethyl L-2-amino-4-phenylbutyrate
46460-23-5, 46460-24-6, 82830-84-0, 124044-66-2

ethyl L-2-amino-4-phenylbutyrate

ethyl 4-phenyl-2-(pyridine-2-sulfonamido)butanoate

ethyl 4-phenyl-2-(pyridine-2-sulfonamido)butanoate

Conditions
ConditionsYield
With pyridine In acetonitrile at 0 - 20℃; for 18h; Inert atmosphere; Sealed tube;97%
pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

dibenzylamine
103-49-1

dibenzylamine

N,N-dibenzyl-pyridine-2-sulfonamide
167958-91-0

N,N-dibenzyl-pyridine-2-sulfonamide

Conditions
ConditionsYield
96%
With potassium carbonate In diethyl ether at 0℃; for 3h;93%
With potassium carbonate In diethyl ether; water at 0℃;
pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

tert-butyl 3-(phenylamino)butanoate
959996-08-8

tert-butyl 3-(phenylamino)butanoate

tert-butyl 3-(N-phenylpyridine-2-sulfonamido)butanoate
959996-28-2

tert-butyl 3-(N-phenylpyridine-2-sulfonamido)butanoate

Conditions
ConditionsYield
With pyridine at 0 - 20℃;96%
pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

benzyl-methyl-amine
103-67-3

benzyl-methyl-amine

N-benzyl-N-methylpyridine-2-sulfonamide

N-benzyl-N-methylpyridine-2-sulfonamide

Conditions
ConditionsYield
95%
With potassium carbonate In diethyl ether; water at 0℃;
pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

D,L-cis-phenylcyclopropylamine
34535-98-3

D,L-cis-phenylcyclopropylamine

N-phenyl-N-cyclopropylpyridine-2-sulfonamide

N-phenyl-N-cyclopropylpyridine-2-sulfonamide

Conditions
ConditionsYield
95%
pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

tert-butyl {[4-fluoro-5-(2-fluoropyridin-3-yl)-1H-pyrrol-3-yl]methyl}methylcarbamate
1055306-88-1

tert-butyl {[4-fluoro-5-(2-fluoropyridin-3-yl)-1H-pyrrol-3-yl]methyl}methylcarbamate

tert-butyl {[4-fluoro-5-(2-fluoropyridin-3-yl)-1-(pyridin-2-ylsulfonyl)-1H-pyrrol-3-yl]methyl}methylcarbamate
1055307-43-1

tert-butyl {[4-fluoro-5-(2-fluoropyridin-3-yl)-1-(pyridin-2-ylsulfonyl)-1H-pyrrol-3-yl]methyl}methylcarbamate

Conditions
ConditionsYield
With 15-crown-5; sodium hydride In tetrahydrofuran at 20℃; for 1h;95%
With 15-crown-5; sodium hydride In tetrahydrofuran at 0℃; for 0.5h;95%
pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

(E)-2-styrylaniline
27652-35-3

(E)-2-styrylaniline

(E)-N-(2-styrylphenyl)pyridine-2-sulfonamide

(E)-N-(2-styrylphenyl)pyridine-2-sulfonamide

Conditions
ConditionsYield
With pyridine at 0 - 25℃; for 2h;95%
pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

hexan-1-ol
111-27-3

hexan-1-ol

Pyridine-2-sulfonic acid hexyl ester

Pyridine-2-sulfonic acid hexyl ester

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0℃;94%
pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

(R)-1-phenyl-ethyl-amine
3886-69-9

(R)-1-phenyl-ethyl-amine

N-(α-Methylbenzyl)pyridine-2-sulfonamide

N-(α-Methylbenzyl)pyridine-2-sulfonamide

Conditions
ConditionsYield
With potassium carbonate In diethyl ether at 0℃; for 1.5h;94%
pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

L-glutamic acid di-tert-butyl ester hydrochloride
32677-01-3

L-glutamic acid di-tert-butyl ester hydrochloride

C18H28N2O6S
1301109-78-3

C18H28N2O6S

Conditions
ConditionsYield
With triethylamine In dichloromethane for 1h;94%
pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

p-toluidine
106-49-0

p-toluidine

N-(p-tolyl)pyridine-2-sulfonamide

N-(p-tolyl)pyridine-2-sulfonamide

Conditions
ConditionsYield
With pyridine In tetrahydrofuran at 0 - 20℃; Inert atmosphere;94%
pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

4-chloro-2-methylbenzeneamine
95-69-2

4-chloro-2-methylbenzeneamine

N-(4-chloro-2-methylphenyl)pyridine-2-sulfonamide

N-(4-chloro-2-methylphenyl)pyridine-2-sulfonamide

Conditions
ConditionsYield
With pyridine In tetrahydrofuran at 0 - 20℃; Inert atmosphere;94%
pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

(S)-Ethyl lactate
687-47-8

(S)-Ethyl lactate

(S)-2-(Pyridine-2-sulfonyloxy)-propionic acid ethyl ester
123455-83-4

(S)-2-(Pyridine-2-sulfonyloxy)-propionic acid ethyl ester

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0℃;93%
pyridine-2-sulfonyl chloride
66715-65-9

pyridine-2-sulfonyl chloride

rac-endo-borneol
6627-72-1

rac-endo-borneol

Pyridine-2-sulfonic acid (1S,2R,4S)-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester
123455-85-6

Pyridine-2-sulfonic acid (1S,2R,4S)-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester

Conditions
ConditionsYield
With triethylamine In dichloromethane at 0℃;93%

Pyridin-2-sulfonyl chloride Specification

The IUPAC name of Pyridin-2-sulfonyl chloride is pyridine-2-sulfonyl chloride. With the CAS registry number 66715-65-9, it is also named as 2-Pyridylsulfonyl chloride. In addition, its molecular formula is C5H4ClNO2S and its molecular weight is 177.60876.

The other characteristics of Pyridin-2-sulfonyl chloride can be summarized as: (1)ACD/LogP: 1.23; (2)# of Rule of 5 Violations: 0; (3)ACD/LogD (pH 5.5): 1.227; (4)ACD/LogD (pH 7.4): 1.227; (5)ACD/BCF (pH 5.5): 5.045; (6)ACD/BCF (pH 7.4): 5.045; (7)ACD/KOC (pH 5.5): 110.843; (8)ACD/KOC (pH 7.4): 110.843; (9)#H bond acceptors: 3; (10)#H bond donors: 0; (11)#Freely Rotating Bonds: 1; (12)Polar Surface Area: 55.41 Å2; (13)Index of Refraction: 1.553; (14)Molar Refractivity: 38.2 cm3; (15)Molar Volume: 119.313 cm3; (16)Polarizability: 15.143×10-24cm3; (17)Surface Tension: 50.296 dyne/cm; (18)Density: 1.489 g/cm3; (19)Flash Point: 125.657 °C; (20)Enthalpy of Vaporization: 50.213 kJ/mol; (21)Boiling Point: 284.162 °C at 760 mmHg; (22)Vapour Pressure: 0.005 mmHg at 25 °C.

People can use the following data to convert to the molecule structure.
(1)SMILES: c1ccnc(c1)S(=O)(=O)Cl
(2)InChI: InChI=1/C5H4ClNO2S/c6-10(8,9)5-3-1-2-4-7-5/h1-4H
(3)InChIKey: JQJOGAGLBDBMLU-UHFFFAOYAI
(4)Std. InChI: InChI=1S/C5H4ClNO2S/c6-10(8,9)5-3-1-2-4-7-5/h1-4H
(5)Std. InChIKey: JQJOGAGLBDBMLU-UHFFFAOYSA-N

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