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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1970013Generated: October 27, 2026

Cyclohexylamine → 8-cyclohexylsulfamoyl-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline-1-carboxylic acid

https://huagongshe.com/reaction/1970013

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclohexylamineHCID 7965—
ReactantTriethylamineHCID 8471—
Reactant8-chlorosulfonyl-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline-1-carboxylic acidHCID 45121068—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product8-cyclohexylsulfamoyl-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline-1-carboxylic acidHCID 6856583344.2%

Reaction Steps

314 μL (2.25 mmol) of triethylamine and 189 μL (1.65 mmol) of cyclohexylamine are added to 490 mg (1.5 mmol) of 8-chlorosulfonyl-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline-1-carboxylic acid suspended in 4 mL of anhydrous dichloromethane and 1 mL of anhydrous dimethylformamide. The reaction mixture is stirred for 2 days at room temperature. The solvents are evaporated, and the residue is taken up in water. The solid is filtered, rinsed with water then diisopropyl ether and dried under vacuum to give 258 mg (44%) of 8-cyclohexylsulfamoyl-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline-1-carboxylic acid in the form of a cream-coloured solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426437B2
Source datasetuspto-grants-2013_04
ORD IDord-29990a8a1f7b4bdd86a486acfff03dd0
Source noteuspto-grants-2013_04