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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300545Generated: October 25, 2026

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

https://huagongshe.com/reaction/2300545

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiazolesulfonyl chlorideHCID 11579235—
Reactant3-{3-[(4-Pyrimidin-2-yl-benzylamino)-methyl]-phenyl}-propionic acid methyl esterHCID 53635220—
SolventTriethylamineHCID 8471—
Product3-(3-{[(4-Pyrimidin-2-yl-benzyl)-(thiazole-2-sulfonyl)-amino]-methyl}-phenyl)-propionic acid methyl esterHCID 54022735—

Reaction Steps

The title compound of Step A was prepared following the method described in Step A of Example 1 from 3-{3-[(4-pyrimidin-2-yl-benzylamino)-methyl]-phenyl}-propionic acid methyl ester, prepared in Step A of Example 11z, and thiazole-2-sulfonyl chloride using triethylamine in place of N,N-diisopropylethylamine. 1H NMR (400 MHz, CDCl3) δ 8.80 (d, 2H), 8.30 (d, 2H), 7.96 (d, 1H), 7.59 (m, 1H), 7.24-7.13 (m, 4H), 7.05 (d, 1H), 6.96 (d, 1H), 6.92 (s, 1H), 4.54 (s, 2H), 4.49 (s, 2H), 3.64 (s, 3H), 2.82 (t, 2H), 2.51 (t, 2H); MS 509 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498172B1
Source datasetuspto-grants-2002_12
ORD IDord-28b2fc0e80a545a69a20305fac1e0b46
Source noteuspto-grants-2002_12