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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1282707Generated: October 31, 2026

Ethanesulfonylchloride, 2-chloro- → HCID 69842640, compound

https://huagongshe.com/reaction/1282707

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanesulfonylchloride, 2-chloro-HCID 15385—
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 178504922HCID 178504922—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
ProductHCID 69842640HCID 69842640116.5%

Reaction Steps

2-Chloroethanesulfonyl chloride (1.85 g, 11.4 mmol) was added to a solution of Compound C of Example 248 (1.0 g, 3.79 mmol) and DIEA (2.6 mL, 15.16 mmol) in dichloromethane (16 mL) at 0° C. under argon. After stirring for 16 hr, the reaction was diluted with chloroform (20 mL) and NaHCO3 (5 mL). The layers were separated, the aqueous layer was extracted with chloroform (2×50 mL). The combined organic extracts were washed with NaHCO3 (2×20 mL) and brine (2×50 mL), dried over MgSO4, filtered and concentrated, to afford Compound A (1.55 g, 116.5%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06455523B1
Source datasetuspto-grants-2002_09
ORD IDord-e474d27757da45809695accda966ef56
Source noteuspto-grants-2002_09