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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266285Generated: October 30, 2026

Methanesulfonyl chloride → HCID 54400977, compound

https://huagongshe.com/reaction/266285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 53906075HCID 53906075—
SolventPyridineHCID 1049—
ProductHCID 54400977HCID 54400977—

Reaction Steps

Methanesulfonyl chloride (hereinafter referred to as mesyl chloride) (96 μl) was added to a solution of (S)-2-(4-chlorobenzenesulfonylamino)-N-(4-ethoxycarbonylphenyl)-3-hydroxypropanamide (132 mg) in pyridine (2.5 ml) and the mixture was stirred for 2 hours at room temperature. The reaction mixture was poured into a saturated saline solution and extracted with ethyl acetate. The combined ethyl acetate layers were washed with saturated saline solution, 1N HCl, and a saturated saline solution, and dried over Na2SO4. Then, the solvent was evaporated under reduced pressure to obtain (S)-2-(4-chlorobenzenesulfonylamino)-N-(4-ethoxycarbonylphenyl)-3-methanesulfonyloxypropanamide (133 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05650428
Source datasetuspto-grants-1997_07
ORD IDord-589c2e7eb9594db1baccf8c80e0dcaf7
Source noteuspto-grants-1997_07