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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 719567Generated: October 31, 2026

Chlorosulfonic acid → HCID 86597376, compound

https://huagongshe.com/reaction/719567

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChlorosulfonic acidHCID 24638—
Reactant[2-(3-Ethyl-4-methyl-2-carbonyl pyrrolidine amido)ethyl]benzeneHCID 86597374—
ProductHCID 86597376HCID 86597376—

Reaction Conditions

Temperature32.5 °C

Reaction Steps

To a cooled (0–5° C.) solution of chlorosulfonic acid (22.4 ml), 4-[2-(3-Ethyl-4-methyl-2-carbonyl pyrrolidineamido)ethyl]benzene (15 gm) was added in small portions over a period of 1 to 2 hrs. Further it was stirred for 30 minutes at this temperature and then temperature was gradually raised to 30 to 35° C. and stirred for 5 hrs. The reaction mixture was quenched into ice-water, and stirred for 1 hr and filtered to obtain the product 4-[2-(3-Ethyl-4-methyl-2-carbonyl pyrrolidineamido)ethyl]benzene sulfonyl chloride (18.8 g). To a cooled (0–5° C.) solution of concentrated ammonia (100 ml), 4[2-(3-Ethyl-4-methyl-2-carbonyl pyrrolidineamido)ethyl]benzene sulfonyl chloride (10 gm) was added in small portions over 30 minutes. The reaction mixture was stirred at this temperature for 30 minutes and then the reaction mixture was allowed to come to room temperature and then stirred for 5 hrs and filtered and dried to obtain 4-[2-(3-Ethyl-4-methyl-2-carbonyl pyrrolidineamido)ethyl]benzene sulfonamide (7.9 gm) having HPLC purity of about 83 to 85%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07132444B2
Source datasetuspto-grants-2006_11
ORD IDord-878fc98189514ebdbc7baf2fa6119f5c
Source noteuspto-grants-2006_11