HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234236Generated: October 30, 2026
Methanesulfonyl chloride → HCID 53664226, compound
https://huagongshe.com/reaction/234236
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 57277465 | HCID 57277465 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 53664226 | HCID 53664226 | 131.9% |
Reaction Steps
A solution of 31 mg of (4R,9S)-16-[dimethyl-(1,1,2-trimethylpropyl)-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-(methylsulfonyloxymethyl)-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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05594135 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-be3955b289504f23b1a732a77004f9b7 |
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| Source note | uspto-grants-1997_01 |
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