HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 423122Generated: October 30, 2026
Methanesulfonyl chloride → Tert-butyl 1-(4-chlorophenyl)-3-(methylsulfonamido)propylcarbamate
https://huagongshe.com/reaction/423122
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Tert-butyl 3-amino-1-(4-chlorophenyl)propylcarbamate | HCID 24729697 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Tert-butyl 1-(4-chlorophenyl)-3-(methylsulfonamido)propylcarbamate | HCID 57750293 | 72.2% |
Reaction Steps
Methanesulfonyl chloride (0.082 mL, 1.05 mmol) was added dropwise to tert-butyl 3-amino-1-(4-chlorophenyl)propylcarbamate (Intermediate 25) (300 mg, 1.05 mmol) and N,N-diisopropylethylamine (0.367 mL, 2.11 mmol) in DCM (4 mL) at 20° C. The resulting solution was stirred at 20° C. for 18 hours. The reaction mixture was concentrated and diluted with Et2O (25 mL) and washed with water (25 mL). The organic layer was dried over MgSO4, filtered and evaporated to afford crude product. The crude product was purified by flash silica chromatography, elution gradient 0 to 20% EtOAc in DCM. Pure fractions were evaporated to dryness to afford tert-butyl 1-(4-chlorophenyl)-3-(methylsulfonamido)propylcarbamate (275 mg, 71.9%) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08101623B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-21df19567c3142a1b552fbd80c89771c |
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| Source note | uspto-grants-2012_01 |
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