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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261760Generated: November 2, 2026

Ethanol → 4-(5-Tert-butyl-1,3,4-thiadiazol-2-ylcarbamoylmethyl)-2-aminothiazole

https://huagongshe.com/reaction/261760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium BicarbonateHCID 516892—
ReactantThioureaHCID 2723790—
ReactantN-(5-tert-butyl-1,3,4-thiadiazol-2-yl)-4-bromoacetoacetamideHCID 21321151—
SolventWaterHCID 962—
Product4-(5-Tert-butyl-1,3,4-thiadiazol-2-ylcarbamoylmethyl)-2-aminothiazoleHCID 2132114896.2%

Reaction Steps

A reaction mixture comprising 11.2 g (0.035 mole) of N-(5-tert-butyl-1,3,4-thiadiazol-2-yl)-4-bromoacetoacetamide, 200 ml of ethanol and 2.8 g (0.037 mole) of thiourea was refluxed for three hours. The reaction solution was cooled and added to 300 ml of water. With stirring, there was slowly added an excess of saturated aqueous sodium bicarbonate. The product was collected and dried. There was obtained 10 g (96.2%) of white solid, m.p. 226° (dec.). N.M.R. (dimethyl-d6 sulfoxide) ∂ 1.4 [C(CH3)3 ], 3.6 (CH2), 6.3 (hetero-aromatic), 6.9 (NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04152329
Source datasetuspto-grants-1979_05
ORD IDord-7c946d3f454f483489af2b83430ccd06
Source noteuspto-grants-1979_05