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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1862806Generated: November 4, 2026

Butylamine → N-Butyl-3-methyl-1,2,4-thiadiazol-5-amine

https://huagongshe.com/reaction/1862806

Reaction equation

Participants

RoleNameHCIDCharge
ReactantButylamineHCID 8007—
Reactant5-Chloro-3-methyl-1,2,4-thiadiazoleHCID 12919159—
SolventEthanolHCID 702—
ProductN-Butyl-3-methyl-1,2,4-thiadiazol-5-amineHCID 20393662—

Reaction Steps

5-Chloro-3-methyl-1,2,4-thiadiazole (27 g, 0.20 mol) was dissolved in 200 ml ethanol and, under cooling in an ice bath, added to an ethanolic solution of butylamine (44 g, 0.60 mol), stirred at room temperature overnight and evaporated to small bulk. Upon addition of ether a white precipitate of butylamine hydrochloride formed which was filtered off. The yellow filtrate was washed with water, dried over magnesium sulphate, filtered and evaporated to dryness to yield a yellow oil which was distilled under vacuum to give 5-butylamino-3-methyl-1,2,4-thiadiazole as a pale yellow liquid. Yield 29.9 g, (87.2%), b.p. 101°-102° C./0.14 mmHg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04166818
Source datasetuspto-grants-1979_09
ORD IDord-433ab213b2df4363a0e5acc0e66b0784
Source noteuspto-grants-1979_09