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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2403202Generated: October 31, 2026

Methanesulfonyl chloride → HCID 71711232, compound

https://huagongshe.com/reaction/2403202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 71711171HCID 71711171—
ProductHCID 71711232HCID 7171123295.4%

Reaction Steps

To a solution of (2S,4R)-4-(2-chlorophenylsulfonyl)-N-(1-cyanocyclopropyl)-1-(1-(piperazin-1-yl)cyclopropanecarbonyl)pyrrolidine-2-carboxamide (35.4 mg, 70 μmol) in methylenehloride (0.7 mL) was added under stirring ethyldiisopropyl amine (18.3 μL, 105 μmol) and methanesulfonyl chloride (6.00 μL, 77.0 μmol). The reaction was stirred at room temperature for 5 hours and additional ethyldiisopropyl amine (18.3 μL, 105 μmol) and methanesulfonyl chloride (6.00 μL, 77.0 μmol) was added. The reaction was stirred at room temperature over night. The reaction was purified by column chromatography on silica gel using ethyl acetate as solvent to yield the title compound as a yellow solid (39 mg, 95%). MS ISP (m/e): 584.1/586.1 (100/44) [(M+H)]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08802665B2
Source datasetuspto-grants-2014_08
ORD IDord-32458d633d3048eca366adaf028624b7
Source noteuspto-grants-2014_08