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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300536Generated: October 29, 2026

3-Chlorobenzenesulphonyl chloride → (3-{[(3-Chloro-benzenesulfonyl)-(4-thiazol-2-yl-benzyl)-amino]-methyl}-phenoxy)-acetic acid tert-butyl ester

https://huagongshe.com/reaction/2300536

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Chlorobenzenesulphonyl chlorideHCID 17909—
ReactantSulfuryl chlorideHCID 24648—
Reactant{3-[(4-Thiazol-2-yl-benzylamino)-methyl]-phenoxy}-acetic Acid Tert-butyl EsterHCID 53752425—
SolventDichloromethaneHCID 6344—
Product(3-{[(3-Chloro-benzenesulfonyl)-(4-thiazol-2-yl-benzyl)-amino]-methyl}-phenoxy)-acetic acid tert-butyl esterHCID 54528990—

Reaction Steps

The title compound of Step A was prepared following the method described in Step A of Example 13w from {3-[(4-thiazol-2-yl-benzylamino)-methyl]-phenoxy}-acetic acid tert-butyl ester, prepared in Step A for Example 13i, and 3-chlorobenzenesulfonyl chloride with the following exception. The sulfonyl chloride was dissolved in CH2Cl2 (1 mL) and 0.28 mL was added to the reaction mixture. MS 585 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498172B1
Source datasetuspto-grants-2002_12
ORD IDord-94021efba707440391c4e8974c718490
Source noteuspto-grants-2002_12