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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 496641Generated: October 29, 2026

Triethylamine → 2(N-methoxy-N-methylcarbamoyl)-3-methansulfonyloxypyrrolidine

https://huagongshe.com/reaction/496641

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 57194245HCID 57194245—
SolventDichloromethaneHCID 6344—
Product2(N-methoxy-N-methylcarbamoyl)-3-methansulfonyloxypyrrolidineHCID 86759849138.8%

Reaction Conditions

Temperature0 °C

Reaction Steps

Methane sulphonyl chloride (3.49 g) was added dropwise over 10 minutes to a mixture of compound 65 (7.6 g) and triethylamine (7.7 ml) in dichloromethane (350 ml) and cooled to 0° C. under an argon atmosphere. It was then stirred at 0° C. for another hour. The reation mixture was then applied directly to a silica flash column which was eluted with ethyl acetate to give (2S,3 S)-1-tert-butoxycarbonyl)-2(N-methoxy-N-methylcarbamoyl)-3-methansulfonyloxypyrrolidine (compound 66) as a gum (9.7 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06946468B1
Source datasetuspto-grants-2005_09
ORD IDord-691c730c0dbb4d2c8591f51f8d5319e7
Source noteuspto-grants-2005_09