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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1034184Generated: October 25, 2026

6-Chloro-N-methyl-3-pyridinemethanamine → 4-[N-(2-chloro-5-pyridylmethyl)-N-methylamino]-3-methyl-5-nitro-2-thiazolone

https://huagongshe.com/reaction/1034184

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Chloro-N-methyl-3-pyridinemethanamineHCID 11094883—
Reactant3-Methyl-4-methylthio-5-nitro-2-thiazoloneHCID 15030462—
SolventEthanolHCID 702—
Product4-[N-(2-chloro-5-pyridylmethyl)-N-methylamino]-3-methyl-5-nitro-2-thiazoloneHCID 1503046391.7%

Reaction Steps

A mixture consisting of 3-methyl-4-methylthio-5-nitro-2-thiazolone (1.0 g), N-(2-chloro-5-pyridylmethyl)-N-methylamine (0.9 g) and ethanol (30 ml) was heat-refluxed for five hours and then cooled to room temperature to obtain the desired 4-[N-(2-chloro-5-pyridylmethyl)-N-methylamino]-3-methyl-5-nitro-2-thiazolone (1.4 g) having a melting point in the range from 147° to 148° C. in a crystal form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05314897
Source datasetuspto-grants-1994_05
ORD IDord-87d158fca10f4a91844c1c6abff059e0
Source noteuspto-grants-1994_05