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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1250864Generated: October 30, 2026

Benzenesulfonyl chloride → HCID 57041896, compound

https://huagongshe.com/reaction/1250864

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-[4-((2S)-2-amino-2-tert-butoxycarbonyl-ethyl)-phenoxy]-butyric acidHCID 69922785—
SolventDimethylformamideHCID 6228—
ProductHCID 57041896HCID 57041896—

Reaction Conditions

Temperature0 °C

Reaction Steps

224.5 mg of 4-[4-((2S)-2-amino-2-tert-butoxycarbonyl-ethyl)-phenoxy]-butyric acid were dissolved in 2 ml of DMF and cooled to 0° C. 207 mg of benzenesulfonyl chloride and 303 mg of diisopropylethylamine were added and the reaction mixture was stirred at 0° C. for 2 hours. The reaction mixture was cooled to −25° C. for 16 hours and then warmed to room temperature. The reaction was quenched by the addition of water, and the mixture was extracted three times with dichloromethane. The combined organic phases were dried with sodium sulfate, filtered and the solvent was removed in vacuo. The residue was chromatographed on silica gel eluting with dichloromethane/methanol/water/acetic acid (9/1/0.1/0.1). Yield 98 mg. MS (ES+): m/e=464.1 (M+H)+; 408.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06340679B1
Source datasetuspto-grants-2002_01
ORD IDord-18f9cfacb862436ebe47848c4cde73a6
Source noteuspto-grants-2002_01