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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Benzyl{[(1R,2R,5S)-5-(dimethylcarbamoyl)-2-hydroxycyclohexyl]sulfamoyl}carbamate | HCID 118671018 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | (1R,2R,4S)-2-{[(Benzyloxycarbonyl) sulfamoyl]amino}-4-(dimethylcarbamoyl)cyclohexyl methanesulfonate | HCID 118661230 | 72% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09447118B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-25067822fe3f4882b79d0365559895f8 |
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| Source note | uspto-grants-2016_09 |
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