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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1697732Generated: November 1, 2026

Water → (3S,5S)-1-(1-(4-chlorophenyl)cyclopropanecarbonyl)-5-(1-cyanocyclopropylcarbamoyl)pyrrolidin-3-yl Benzenesulfonate

https://huagongshe.com/reaction/1697732

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantTriethylamineHCID 8471—
Reactant(2S,4S)-1-(1-(4-chlorophenyl)cyclopropanecarbonyl)-N-(1-cyanocyclopropyl)-4-hydroxypyrrolidine-2-carboxamideHCID 67278484—
Catalyst2-DimethylaminopyridineHCID 21885—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product(3S,5S)-1-(1-(4-chlorophenyl)cyclopropanecarbonyl)-5-(1-cyanocyclopropylcarbamoyl)pyrrolidin-3-yl BenzenesulfonateHCID 8664686799.2%

Reaction Conditions

Temperature2.5 °C

Reaction Steps

To a solution of (2S,4S)-1-(1-(4-chlorophenyl)cyclopropanecarbonyl)-N-(1-cyanocyclopropyl)-4-hydroxypyrrolidine-2-carboxamide (Example 457b; 5 g) in tetrahydrofuran (22 mL) at 0-5° C., was added benzenesulfonyl chloride (2.89 g, 2.1 ml, 16.2 mmol, Eq: 1.21), dimethylaminopyridine (88.7 mg) and triethylamine (2.41 g) within 5 minutes. The mixture was stirred at 0-5° C. for 15 min, then at 22° C. for 22 hr. Water (6.7 mL) and methanol (15.6 mL) were added at 0-5° C. and the mixture was concentrated in vacuo to afford a gum. This gum was washed with methanol and dried in vacuo to yield 6.82 g (99%) of the title compound as a light brown foam. MS (ESI): m/z=531.15 [M+NH4]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163793B2
Source datasetuspto-grants-2012_04
ORD IDord-c68e94f45c5644c993b29b1f51ee7851
Source noteuspto-grants-2012_04