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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300544Generated: October 29, 2026

2-Thiazolesulfonyl chloride → 3-(3-{[(4-tert-Butyl-benzyl)-(thiazole-2-sulfonyl)-amino]-methyl}-phenyl)-propionic acid methyl ester

https://huagongshe.com/reaction/2300544

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiazolesulfonyl chlorideHCID 11579235—
Reactant3-{3-[(4-tert-Butyl-benzylamino)-methyl]-phenyl}-propionic acid methyl esterHCID 54364343—
SolventTriethylamineHCID 8471—
Product3-(3-{[(4-tert-Butyl-benzyl)-(thiazole-2-sulfonyl)-amino]-methyl}-phenyl)-propionic acid methyl esterHCID 54191571—

Reaction Steps

The title compound of Step A was prepared following the method described in Step A of Example 1 from 3-{3-[(4-tert-butyl-benzylamino)-methyl]-phenyl}-propionic acid methyl ester, prepared in Step A of Example 12s, and thiazole-2-sulfonyl chloride using triethylamine in place of N,N-diisopropylethylamine. 1H NMR (400 MHz, CDCl3) δ 7.93 (d, 1H), 7.56 (d, 1H), 7.23 (d, 2H), 7.14 (m, 1H), 7.04 (m, 3H), 6.98 (m, 2H), 4.47 (s, 2H), 4.41 (s, 2H), 3.67 (s, 3H), 2.84 (t, 2H), 2.54 (t, 2H), 1.27 (s, 9H); MS 487 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498172B1
Source datasetuspto-grants-2002_12
ORD IDord-71821327583541538c918bb94e0d88cc
Source noteuspto-grants-2002_12