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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300489Generated: October 30, 2026

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

https://huagongshe.com/reaction/2300489

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridine-2-sulfonyl chloride hydrochlorideHCID 13791306—
Reactant3-{3-[(4-tert-Butyl-benzylamino)-methyl]-phenyl}-propionic acid methyl esterHCID 54364343—
SolventTriethylamineHCID 8471—
Product3-(3-{[(4-tert-Butyl-benzyl)-(pyridine-2-sulfonyl)-amino]-methyl}-phenyl)-propionic acid methyl esterHCID 53733186—

Reaction Steps

The title compound of Step B was prepared following the method described in Step B of Example 1 from 3-{3-[(4-tert-butyl-benzylamino)-methyl]-phenyl}-propionic acid methyl ester of Step A and pyridine-2sulfonyl chloride hydrochloride, of Preparation 47 using triethylamine in place of N,N-diisopropylethylamine. 1H NMR (400 MHz, CDCl3) δ 8.62 (m, 1H), 7.90 (m, 1H), 7.81 (m, 1H), 7.41 (m, 1H), 7.17 (d, 2H), 7.09 (m, 1H), 6.99 (m, 3H), 6.92 (m, 2H), 4.48 (s, 2H), 4.43 (s, 2H), 3.65 (s, 3H), 2.80 (t, 2H), 2.51 (t, 2H), 1.24 (t, 9H); MS 481 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498172B1
Source datasetuspto-grants-2002_12
ORD IDord-5ef76b2407e341d5b3f7a1b5184a2b19
Source noteuspto-grants-2002_12