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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 591192Generated: October 26, 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/591192

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 numberUS09238619B2
Source datasetuspto-grants-2016_01
ORD IDord-dca7e62cc8f248f3b4e8aeecc4c1aa90
Source noteuspto-grants-2016_01