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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2290363Generated: November 2, 2026

HCID 20232011, compound → HCID 15586410, compound

https://huagongshe.com/reaction/2290363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 20232011HCID 20232011—
ReactantHCID 20232073HCID 20232073—
Solvent1-ButanolHCID 263—
ProductHCID 15586410HCID 1558641017%

Reaction Steps

A mixture of 6-(4-chlorophenyl)-3-hydrazino-5-methyl-1,2,4-triazine (7 g), 2-iodomethylthio-2-imidazoline (8.11 g) and n-butanol (50 ml) was refluxed for 3 hours with stirring. After cooling, the mixture was evaporated under reduced pressure and the residue was dissolved in 1N hydrochloric acid. The solution was washed with ethyl acetate and made alkaline with an aqueous solution of potassium carbonate. The resultant precipitates were collected by filtration, washed with water, dried and recrystallized from methanol and then from ethanol to give dark red crystals of 6-(4-chlorophenyl)-3-[2-(2-imidazolin-2-yl)hydrazino]-5-methyl-1,2,4-triazine (1.53 g), m.p. 230°~231° C. (decomp.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04616014
Source datasetuspto-grants-1986_10
ORD IDord-62ab3297fbc64afdbb932da8de2854f1
Source noteuspto-grants-1986_10