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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1156404Generated: October 31, 2026

1,3,4-Thiadiazol-2-amine → HCID 13002953, compound

https://huagongshe.com/reaction/1156404

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3,4-Thiadiazol-2-amineHCID 19909—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 20536095HCID 20536095—
SolventEthanolHCID 702—
ProductHCID 13002953HCID 1300295371.9%

Reaction Steps

Ten grams of 2-amino-1,3,4-thiadiazole, 16.6 g of 1-(2-chloroethyl)-3-nitrourea and 84 g of sodium hydrogencarbonate were stirred in 100 ml of diluted ethanol at a temperature of 80° C. for 2 hours. While being still hot after the reaction, the precipitated inorganic matters were removed by filtration, and the filtrate was cooled. The precipitated crystals were collected by filtration and washed with water, to obtain 14.7 g (Yield 71%) of 2-{3-(2-chloroethyl)ureido}-1,3,4-thiadiazole. The product was then treated in the same manner as in Example 1 (2), to obtain 2-{3-(2-chloroethyl)-3-nitrosoureido}-1,3,4-thiadiazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04335247
Source datasetuspto-grants-1982_06
ORD IDord-a95e07fce2f24b25a51c4996fb4aae03
Source noteuspto-grants-1982_06