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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657032Generated: November 1, 2026

2-Chloro-5-aminomethylthiazole → 1-(1-Chloroethoxycarbonyl)-3-(2-chloro-5-thiazolylmethyl)-1-methyl-2-nitroguanidine

https://huagongshe.com/reaction/1657032

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloro-5-aminomethylthiazoleHCID 10154129—
ReactantN-(1-chloroethoxycarbonyl)-S,N-dimethyl-N'-nitroisothioureaHCID 73653905—
SolventChloroformHCID 6212—
Product1-(1-Chloroethoxycarbonyl)-3-(2-chloro-5-thiazolylmethyl)-1-methyl-2-nitroguanidineHCID 13633150138.7%

Reaction Conditions

Temperature-20 °C

Reaction Steps

To a stirred solution of N-(1-chloroethoxycarbonyl)-S,N-dimethyl-N'-nitroisothiourea (6.50 g) in CHCl3 (15 ml) was added a solution of 2-chloro-5-thiazolylmethylamine (3.78 g) in CHCl3 (5 ml) dropwise below -20° C. over 20 minutes. After stirring at -20° C. for 30 minutes, insolubles were removed by filtration and the filtrate was concentrated in vacuo. The residue was applied to column chromatography on silica gel. The column was eluted with hexane-AcOEt (1:1) to afford 3.50 g of 1-(1-chloroethoxycarbonyl)-3-(2-chloro-5-thiazolylmethyl)-1-methyl-2-nitroguanidine (Compound No. 12) as an orange oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05256679
Source datasetuspto-grants-1993_10
ORD IDord-aed818bb104d487aaca0b5a48d7700ef
Source noteuspto-grants-1993_10