2-Mercaptopyridine
pyridine-2-sulfonyl chloride
Conditions | Yield |
---|---|
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
A
2-chloropyridine
B
pyridine-2-sulfonyl chloride
Conditions | Yield |
---|---|
With 1,3-dichloro-5,5-dimethylhydantoin; acetic acid In dichloromethane; water at 0 - 20℃; Inert atmosphere; | A 20% B 78% |
Conditions | Yield |
---|---|
With N-chloro-succinimide In water; acetonitrile at 35℃; for 0.25h; | A 11% B 57% |
2-Mercaptopyridine
hydrogenchloride
chlorine
pyridine-2-sulfonyl chloride
2-bromo-pyridine
pyridine-2-sulfonyl chloride
Conditions | Yield |
---|---|
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℃; |
Conditions | Yield |
---|---|
In hydrogenchloride |
Conditions | Yield |
---|---|
With conc HCl In dichloromethane; water |
2-Mercaptopyridine
pyridine-2-sulfonyl chloride
Conditions | Yield |
---|---|
With sulfuric acid; chlorine |
2,2'-dipyridyldisulphide
pyridine-2-sulfonyl chloride
Conditions | Yield |
---|---|
With hydrogenchloride; chlorine at -10 - -8℃; for 0.5h; | |
With hydrogenchloride; chlorine In water at -10℃; for 0.5h; |
2-pyridinesulfinic acid sodium salt
pyridine-2-sulfonyl chloride
Conditions | Yield |
---|---|
With N-chloro-succinimide In dichloromethane |
2-pyridinesulfonyl chloride hydrochloride
pyridine-2-sulfonyl chloride
Conditions | Yield |
---|---|
In dichloromethane |
pyridine-2-sulfonyl chloride
2-Benzyloxyethanol
Pyridine-2-sulfonic acid 2-benzyloxy-ethyl ester
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0℃; | 99% |
pyridine-2-sulfonyl chloride
((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
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0℃; | 99% |
Conditions | Yield |
---|---|
With triethylamine In water; ethyl acetate | 99% |
Conditions | Yield |
---|---|
Stage #1: C16H13NO With sodium hydride In tetrahydrofuran at 0℃; Stage #2: pyridine-2-sulfonyl chloride In tetrahydrofuran at 0 - 20℃; | 99% |
piperidine
pyridine-2-sulfonyl chloride
Piperidin-1-yl pyridin-2-yl sulfone
Conditions | Yield |
---|---|
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
3-bromopropylamine hydrochloride
N-(3-bromopropyl)-pyridine-2-sulfonamide
Conditions | Yield |
---|---|
With potassium carbonate In dichloromethane; water at 0℃; for 1h; | 98% |
Conditions | Yield |
---|---|
With potassium carbonate In diethyl ether at 0℃; for 1.5h; | 98% |
pyridine-2-sulfonyl chloride
benzylamine
pyridine-2-sulfonic acid benzylamide
Conditions | Yield |
---|---|
With triethylamine In dichloromethane | 98% |
86% |
pyridine-2-sulfonyl chloride
L-valine methylester hydrochloride
(S)-mehyl 3-mehyl-2-(pyridine-2-sulfonamido)butanoate
Conditions | Yield |
---|---|
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
non-1-yn-3-ol
Pyridine-2-sulfonic acid 1-ethynyl-heptyl ester
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0℃; | 97% |
pyridine-2-sulfonyl chloride
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
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0℃; | 97% |
pyridine-2-sulfonyl chloride
L-phenylalanine tert-butyl ester
Conditions | Yield |
---|---|
With potassium carbonate In diethyl ether at 0℃; for 6h; | 97% |
pyridine-2-sulfonyl chloride
C17H16N2O3S
Conditions | Yield |
---|---|
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
pyridine-2-sulfonyl chloride
2-(pyrrolidin-1-ylsulfonyl)pyridine
Conditions | Yield |
---|---|
In dichloromethane at 0 - 25℃; for 12h; Inert atmosphere; | 97% |
In dichloromethane at 20℃; Cooling with ice; |
pyridine-2-sulfonyl chloride
ethyl L-2-amino-4-phenylbutyrate
Conditions | Yield |
---|---|
With pyridine In acetonitrile at 0 - 20℃; for 18h; Inert atmosphere; Sealed tube; | 97% |
pyridine-2-sulfonyl chloride
dibenzylamine
N,N-dibenzyl-pyridine-2-sulfonamide
Conditions | Yield |
---|---|
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
tert-butyl 3-(phenylamino)butanoate
tert-butyl 3-(N-phenylpyridine-2-sulfonamido)butanoate
Conditions | Yield |
---|---|
With pyridine at 0 - 20℃; | 96% |
pyridine-2-sulfonyl chloride
benzyl-methyl-amine
Conditions | Yield |
---|---|
95% | |
With potassium carbonate In diethyl ether; water at 0℃; |
pyridine-2-sulfonyl chloride
D,L-cis-phenylcyclopropylamine
Conditions | Yield |
---|---|
95% |
pyridine-2-sulfonyl chloride
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
Conditions | Yield |
---|---|
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
(E)-2-styrylaniline
Conditions | Yield |
---|---|
With pyridine at 0 - 25℃; for 2h; | 95% |
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0℃; | 94% |
pyridine-2-sulfonyl chloride
(R)-1-phenyl-ethyl-amine
Conditions | Yield |
---|---|
With potassium carbonate In diethyl ether at 0℃; for 1.5h; | 94% |
pyridine-2-sulfonyl chloride
L-glutamic acid di-tert-butyl ester hydrochloride
C18H28N2O6S
Conditions | Yield |
---|---|
With triethylamine In dichloromethane for 1h; | 94% |
Conditions | Yield |
---|---|
With pyridine In tetrahydrofuran at 0 - 20℃; Inert atmosphere; | 94% |
pyridine-2-sulfonyl chloride
4-chloro-2-methylbenzeneamine
Conditions | Yield |
---|---|
With pyridine In tetrahydrofuran at 0 - 20℃; Inert atmosphere; | 94% |
pyridine-2-sulfonyl chloride
(S)-Ethyl lactate
(S)-2-(Pyridine-2-sulfonyloxy)-propionic acid ethyl ester
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0℃; | 93% |
pyridine-2-sulfonyl chloride
rac-endo-borneol
Pyridine-2-sulfonic acid (1S,2R,4S)-1,7,7-trimethyl-bicyclo[2.2.1]hept-2-yl ester
Conditions | Yield |
---|---|
With triethylamine In dichloromethane at 0℃; | 93% |
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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