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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173110Generated: November 2, 2026

4-(Chlorosulfonyl)benzoic acid → HCID 10641632, compound

https://huagongshe.com/reaction/1173110

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(Chlorosulfonyl)benzoic acidHCID 82385—
Reactant3-chloro-1H-indol-7-amineHCID 11008290—
SolventPyridineHCID 1049—
ProductHCID 10641632HCID 1064163277.8%

Reaction Steps

2.82 g (12.8 mmol) of 4-(chlorosulfonyl)benzoic acid and 1.42 g (8.54 mmol) of 7-amino-3-chloro-1H-indole were reacted with each other in pyridine at room temperature under stirring overnight, to give 2.33 g of 4-[N-(3-chloro-1H-indole-7-yl)sulfamoyl]benzoic acid. To 303 mg (0.86 mmol) of the product were successively added 260 μl of dimethylformamide, 204 μl (0.95 mmol) of diphenylphosphorylazide, 132 μl (0.95 mmol) of triethylamine and 113 μl (0.94 mmol) of 2-(2-aminoethyl)pyridine, followed by stirring at room temperature overnight. After concentrating, ethyl acetate and an aqueous saturated sodium bicarbonate were added thereto. The organic layer was separated and washed with brine. After evaporating the solvent, the residue was purified by silica gel column chromatography, to give 175 mg of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834049B2
Source datasetuspto-grants-2010_11
ORD IDord-4fb1ec3fa2a048a7b304202f3bf1c34c
Source noteuspto-grants-2010_11