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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1112052Generated: November 2, 2026

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

https://huagongshe.com/reaction/1112052

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 3 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 numberUS04120690
Source datasetuspto-grants-1978_10
ORD IDord-40cad29f07be48fa868827efc45535fd
Source noteuspto-grants-1978_10