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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1082173Generated: November 1, 2026

Methanesulfonyl chloride → HCID 53664226, compound

https://huagongshe.com/reaction/1082173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 57277465HCID 57277465—
SolventPyridineHCID 1049—
ProductHCID 53664226HCID 53664226131.9%

Reaction Steps

A solution of 31 mg of (4R,9S)-16-[dimethyl-(1,1,2-trimethyl-propyl)-silanyloxy]-9-hydroxymethyl-14-methoxy-13-methyl-4-(3-methyl -1,2,4-oxadiazol-5-yl)-6-thioxo-1,3,4,5,6,7,8,9, 10,12-decahydro-11,2,5-benzoxathiaazacyclotetradecin-12-one and 11.5 mg of methanesulfonyl chloride in 0.2 ml of pyridine was stirred at 20° C. for 3 h. The solution was partitioned between dichloromethane and 1M aqueous oxalic acid. The organic layer was washed with brine, dried over sodium sulfate and evaporated in vacuo to yield 46 mg of (4R,9R)-16-[dimethyl-(1,1,2-trimethyl-propyl) -silanyloxy]-14-methoxy-13-methyl-4-(3-methyl-1,2,4-oxadiazol-5-yl)-9-(methyl -sulfonyloxymethyl)-6-thioxo-1,3,4,5,6,7,8,9,10,12-decahydro-11,2,5-benzoxathiaazacyclotetradecin-12-one as an amorphous solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05589473
Source datasetuspto-grants-1996_12
ORD IDord-35892843fb5644dc8af626b3b019ad64
Source noteuspto-grants-1996_12