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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 611533Generated: October 30, 2026

Water → N-[4-(4-chloro-7-isopropylpyrrolo[2,3-d]pyrimidin-5-yl)phenyl]benzenesulphonamide

https://huagongshe.com/reaction/611533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantTriethylamineHCID 8471—
Reactant5-(4-Aminophenyl)-4-chloro-7-isopropylpyrrolo[2,3-d]pyrimidineHCID 19597487—
SolventDichloromethaneHCID 6344—
ProductN-[4-(4-chloro-7-isopropylpyrrolo[2,3-d]pyrimidin-5-yl)phenyl]benzenesulphonamideHCID 19597404—

Reaction Conditions

Temperature0 °C

Reaction Steps

Benzenesulphonyl chloride (0.27 g) in dichloromethane (5 ml) was added dropwise with stirring to a solution of 5-(4-aminophenyl)-4-chloro-7-isopropylpyrrolo[2,3-d]pyrimidine (0.40 g) and triethylamine (155 mg) in dichloromethane (15 ml) at 0° C. under nitrogen. The mixture was stirred at 0° C. for one hour and then warmed to ambient temperature and stirred at this temperature for 18 hours. Water (20 ml) was added and the mixture was extracted with dichloromethane. The combined organic layers were washed with sodium bicarbonate, dried, filtered and evaporated to give N-[4-(4-chloro-7-isopropylpyrrolo[2,3-d]pyrimidin-5-yl)phenyl]benzenesulphonamide

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06001839
Source datasetuspto-grants-1999_12
ORD IDord-ec17fdec137f4630aa6d22648b38799b
Source noteuspto-grants-1999_12