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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 373794Generated: October 26, 2026

(2-Chloro-thiazol-5-ylmethyl)-methyl-amine → N-[(2-chloro-5-thiazolyl)methyl]-N-methyl-N'-nitroguanidine

https://huagongshe.com/reaction/373794

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2-Chloro-thiazol-5-ylmethyl)-methyl-amineHCID 22450372—
ReactantN-Nitro-S-methylisothioureaHCID 135927615—
SolventEthanolHCID 702—
ProductN-[(2-chloro-5-thiazolyl)methyl]-N-methyl-N'-nitroguanidineHCID 13602351947.9%

Reaction Steps

A mixture of 1.50 g of 2-chloro-N-methyl-5-thiazolemethanamine, 1.13 g of S-methyl-N-nitroisothiourea and 6 ml of ethanol was heated under reflux for 6 hours. After cooling, the reaction mixture was concentrated under reduced pressure and the residue was purified by silica gel column chromatography (Solvent: Chloroform/Methanol=20/1) to obtain 1.00 g of the title compound as crystals. This compound is No. 6 in Table 1. m.p.: 116.0°-117.0° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05166164
Source datasetuspto-grants-1992_11
ORD IDord-413423d140104099ae13a250c643f00b
Source noteuspto-grants-1992_11