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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64045Generated: October 28, 2026

Dichloromethane → (1R,2R,4S)-2-{[(Benzyloxycarbonyl) sulfamoyl]amino}-4-(dimethylcarbamoyl)cyclohexyl methanesulfonate

https://huagongshe.com/reaction/64045

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantBenzyl{[(1R,2R,5S)-5-(dimethylcarbamoyl)-2-hydroxycyclohexyl]sulfamoyl}carbamateHCID 118671018—
SolventTriethylamineHCID 8471—
Product(1R,2R,4S)-2-{[(Benzyloxycarbonyl) sulfamoyl]amino}-4-(dimethylcarbamoyl)cyclohexyl methanesulfonateHCID 11866123072%

Reaction Conditions

Temperature0 °C

Reaction Steps

Benzyl {[(1R,2R,5S)-5-(dimethylcarbamoyl)-2-hydroxycyclohexyl]sulfamoyl}carbamate (1.00 g) was added to methylene chloride (10 ml), and the obtained solution was then cooled to approximately 0° C. Triethylamine (0.52 ml) was added to the reaction solution, and methanesulfonyl chloride (0.28 ml) was then added dropwise to the mixed solution. The obtained mixture was stirred for approximately 1 hour. The precipitated crystals were collected by filtration, and were then washed with methylene chloride (1 ml). The obtained crystals were dried under reduced pressure to obtain 866 mg of the title compound (yield: 72%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09447118B2
Source datasetuspto-grants-2016_09
ORD IDord-25067822fe3f4882b79d0365559895f8
Source noteuspto-grants-2016_09