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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 331694Generated: October 25, 2026

1-methyl-1H-pyrazole-4-sulfonyl chloride → tert-Butyl {2-[1-(4-chlorophenyl)cyclobutyl]-2-[3-({methyl[(1-methyl-1H-pyrazol-4-yl)sulfonyl]amino}methyl)phenyl]ethyl}carbamate

https://huagongshe.com/reaction/331694

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-methyl-1H-pyrazole-4-sulfonyl chlorideHCID 17024730—
Reactanttert-Butyl (2-[1-(4-chlorophenyl)cyclobutyl]-2-{3-[(methylamino)methyl]phenyl}ethyl)carbamateHCID 68077950—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Producttert-Butyl {2-[1-(4-chlorophenyl)cyclobutyl]-2-[3-({methyl[(1-methyl-1H-pyrazol-4-yl)sulfonyl]amino}methyl)phenyl]ethyl}carbamateHCID 56835836—

Reaction Steps

tert-Butyl (2-[1-(4-chlorophenyl)cyclobutyl]-2-{3-[(methylamino)methyl]phenyl}ethyl)carbamate (35 mg, 0.082 mmol) was dissolved in dichloromethane (0.8 mL). 4-Dimethylaminopyridine (10 mg, 0.082 mmol) and 1-methyl-1H-pyrazole-4-sulfonyl chloride (16 mg, 0.09 mmol) was added. The reaction mixture was stirred at room temperature over night. The reaction mixture was diluted with ethyl acetate (20 ml) and washed with aqueous hydrochloric acid (1 N, 5 ml, twice) and sodium bicarbonate. The organic layer was dried (magnesium sulfate) and concentrated in vacuo. The crude product was purified by preparative thin layer chromatography (silica, ethyl acetate, n-heptane). Yield: 36 mg (0.063 mmol, 77%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877794B2
Source datasetuspto-grants-2014_11
ORD IDord-139465d4a1ca4c4789850d68311ff3be
Source noteuspto-grants-2014_11