HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351270Generated: October 30, 2026
Methanesulfonyl chloride → HCID 86592860, compound
https://huagongshe.com/reaction/351270
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 91605231 | HCID 91605231 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 86592860 | HCID 86592860 | 81.3% |
Reaction Steps
To a solution of tert-butyl{4-[3-(1-hydroxy-1-methyl-ethyl)-1-(4-methoxyphenyl)-1H-pyrazol-5-yl]benzyl}-carbamate (1.1 g) and Et3N (1.02 g) was added methane sulfonyl chloride (576 mg). The mixture was stirred at ambient temperature overnight. The mixture was concentrated in vacuo. The residue was partitioned between AcOEt and 1M HCl. The organic layer was separated, washed with saturated aqueous sodium bicarbonate solution and saturated aqueous sodium chloride solution, dried over magnesium sulfate, and concentrated in vacuo. The residue was purified by silica gel column chromatography eluted with AcOEt/n-hexane=25%. The pure fraction was collected and concentrated in vacuo to give tert-butyl {4-[3-isopropenyl-1-(4-methoxyphenyl)-1-H-pyrazol-5-yl]benzyl}carbamate (857 mg) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07183306B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-829e12dd1f7842a691ae85fb024600c3 |
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| Source note | uspto-grants-2007_02 |
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