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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1828155Generated: October 30, 2026

Benzenesulfonyl chloride → (Tert-butyl)[(5-chloro(1,3-thiazol-2-yl))sulfonyl]amine

https://huagongshe.com/reaction/1828155

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
Reactant(Tert-butyl)(1,3-thiazol-2-ylsulfonyl)amineHCID 15813414—
ReactantButyllithiumHCID 178418339—
SolventDiethyl EtherHCID 3283—
SolventEthyl AcetateHCID 8857—
Product(Tert-butyl)[(5-chloro(1,3-thiazol-2-yl))sulfonyl]amineHCID 2206447133%

Reaction Steps

To a solution of (tert-butyl)(1,3-thiazol-2-ylsulfonyl)amine (0.15 g, 0.7 mmol) in ethyl ether (3 mL) at −78° C. was added a 1.6M solution of n-butyllithium (0.875 mL, 1.4 mmol) in hexanes via syringe under argon. The reaction mixture was stirred at −7,8° C. for 1 hr, then neat benzenesulfonyl chloride (90 μL, 0.7 mmol) was added. The resulting suspension was stirred at room temp for 2 hr. The reaction was diluted with EtOAc, washed with water and brine, dried, concentrated in vacuo and chromatographed (15% EtOAc/hexane) to give pure desired compound (58 mg, 33%). ES-MS (M+Na)+=277, 279 (Cl), (M-tBu+H)+=199, 201 (Cl).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07056926B2
Source datasetuspto-grants-2006_06
ORD IDord-54aa06fb649e445380740454a9cb93d3
Source noteuspto-grants-2006_06