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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantDiisopropylethylamineHCID 81531—
ReactantTert-butyl 3-amino-1-(4-chlorophenyl)propylcarbamateHCID 24729697—
SolventDichloromethaneHCID 6344—
ProductTert-butyl 1-(4-chlorophenyl)-3-(methylsulfonamido)propylcarbamateHCID 5775029372.2%

Reaction Conditions

Temperature20 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08101623B2
Source datasetuspto-grants-2012_01
ORD IDord-21df19567c3142a1b552fbd80c89771c
Source noteuspto-grants-2012_01