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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613681Generated: October 29, 2026

N-Methylhydrazinecarbothioamide → 2-[4-Chloro-1-(pyridin-3-yl)-butylidene]-N-methyl-hydrazinecarbothioamide

https://huagongshe.com/reaction/613681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylhydrazinecarbothioamideHCID 2723853—
Reactant4-Chloro-1-(pyridin-3-YL)butan-1-oneHCID 12471005—
SolventEthanolHCID 702—
Product2-[4-Chloro-1-(pyridin-3-yl)-butylidene]-N-methyl-hydrazinecarbothioamideHCID 54474414112.2%

Reaction Steps

A mixture of 4-chloro-1-(3-pyridinyl)-1-butanone (4.4 g, 24 mmol) and 4-methylthiosemicarbazide (2.5 g, 24 mmol) in 150 mL of ethanol under a nitrogen atmosphere was warmed to dissolve all the solids and then allowed to stir at room temperature overnight. By TLC the reaction was not complete. The reaction was then heated at 70° C. for 5 hours and overnight at room temperature. The solvent was removed under reduced pressure to give 7.29 g of a yellow oil. Purification of this oil on 700 g of silica gel (230-400 mesh) using 50-70% EtOAc-hexane as the eluent gave 4.14 g (64%) of the title compound as a white solid, mp 100-102° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06008362
Source datasetuspto-grants-1999_12
ORD IDord-0b3210bde09d4528a1999574f3a04593
Source noteuspto-grants-1999_12