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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 507291Generated: October 25, 2026

4-Chlorobenzenesulfonyl chloride → (2R)-2-(4-Chlorobenzenesulfonylamino)-4-methylpentanoic acid amide

https://huagongshe.com/reaction/507291

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzenesulfonyl chlorideHCID 7398—
ReactantTriethylamineHCID 8471—
Reactant(R)-2-Amino-4-methylpentanamide hydrochlorideHCID 56776963—
SolventDichloromethaneHCID 6344—
Product(2R)-2-(4-Chlorobenzenesulfonylamino)-4-methylpentanoic acid amideHCID 5900105890%

Reaction Steps

To a solution of (D)-leucinamide hydrochloride (0.25 g, 1.5 mmol), and Et3N (0.43 mL, 3.0 mmol) in CH2Cl2 (150 mL) was added 4-chlorobenzenesulfonyl chloride (380 mg, 1.8 mmol). The resulting solution was stirred at rt for 18 h. The reaction was then diluted with CH2Cl2 (200 mL) and washed with H2O, 0.5 N HCl, brine, and dried over MgSO4, to afford the titled compound (410 mg) as a white solid in 90% yield. MS (ESI), (M+H)+ 305.2; 1H NMR (DMSO-d6) δ 7.77 (d, 2H, J=8.7), 7.62 (d, 2H, J=8.7), 6.90 (br s, 1H), 3.67 (m, 1H), 1.54 (m, 1H), 1.31 (m, 2H), 0.81 (d, 3H, J=7.0), 0.71 (d, 3H, J=7.0).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07786122B2
Source datasetuspto-grants-2010_08
ORD IDord-9bb8f87368bb4c3da831aca7229eeb11
Source noteuspto-grants-2010_08