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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2218583Generated: October 30, 2026

4-Chloro-5-methoxy-benzothiazole-2-sulfonyl chloride → [2-(4-Chloro-5-methoxy benzothiazole-2-sulfonylamino)-ethyl]-glycine ethyl ester

https://huagongshe.com/reaction/2218583

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chloro-5-methoxy-benzothiazole-2-sulfonyl chlorideHCID 21868445—
ReactantN-beta-Aminoethyl-gly-oet 2hclHCID 74889816—
Product[2-(4-Chloro-5-methoxy benzothiazole-2-sulfonylamino)-ethyl]-glycine ethyl esterHCID 2186841189%

Reaction Steps

The title compound (726 mg, 89%) was synthesized by the reaction of N-(2-aminoethyl)-glycine ethyl ester 2HCl (398 mg, 2.0 mmol) with 4-chloro-5-methoxy-benzothiazole-2-sulfonyl chloride (596 mg, 2.0 mmol) as per the procedure of Example 1. 1H NMR (500 MHz; DMSO-d6) δ 8.18 (d, 1H), 7.57 (d, 1H), 4.00 (q, 2H), 3.97 (s, 3H), 3.22 (s, 2H), 3.14 (t, 2H), 2.62 (t, 2H), 1.13 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07411065B2
Source datasetuspto-grants-2008_08
ORD IDord-96604bedf55149c3ba22f9b772168f55
Source noteuspto-grants-2008_08