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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2204980Generated: October 31, 2026

Pyridine → (R)-tert-butyl 2-(benzyloxycarbonylamino)-3-((S)-2,3-bis(methylsulfonyloxy)propylthio)-propanoate

https://huagongshe.com/reaction/2204980

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant(R)-tert-butyl 2-(benzyloxycarbonylamino)-3-((S)-2,3-dihydroxypropylthio)propanoateHCID 67402221—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product(R)-tert-butyl 2-(benzyloxycarbonylamino)-3-((S)-2,3-bis(methylsulfonyloxy)propylthio)-propanoateHCID 86678279—

Reaction Steps

A solution of (R)-tert-butyl 2-(benzyloxycarbonylamino)-3-((S)-2,3-dihydroxypropylthio)propanoate (1 eq) was stirred in dry DCM (0.1M) in an ice bath (0° C.) under an atmosphere of N2. Pyridine (8.0 eq) was then carefully added at 0° C. Methanesulfonyl chloride (4.0 eq) and DMAP (0.1 eq) were added with the reaction slowly warming to room temperature, then stirred overnight. The crude reaction mixture was then loaded directly onto a silica column and purified by flash chromatography on a COMBIFLASH® system (ISCO) using a gradient of 100% Hex, 0-20% EtOAc/Hex, 20-50% EtOAc/Hex, 100% EtOAc to afford the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365506B2
Source datasetuspto-grants-2016_06
ORD IDord-7523995fc7a444549968be0aa390c7b6
Source noteuspto-grants-2016_06