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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261761Generated: October 26, 2026

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

https://huagongshe.com/reaction/261761

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium BicarbonateHCID 516892—
ReactantMethylthioureaHCID 2723704—
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-methylaminothiazoleHCID 2132115987.2%

Reaction Steps

A reaction mixture containing 11.4 g (0.035 mole) of N-(5-tert-butyl-1,3,4-thiadiazol-2-yl)-4-bromoacetoacetamide, 150 ml of ethanol and 3.3 g (0.036 mole) of N-methylthiourea was refluxed for four hours. The reaction solution was poured into 300 ml of water and treated with excess aqueous sodium bicarbonate. The product was isolated and dried. There was obtained 9.5 g (87.2%) of white solid, m.p. 198°-200° (dec.). N.M.R. (CDCl3) ∂ 1.4 [C(CH3)3 ], 3.0 (CH3), 3.8 (CH2), 6.4 (hetero-aromatic).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04152329
Source datasetuspto-grants-1979_05
ORD IDord-d582eac5f7a14c52b888cef17df73c51
Source noteuspto-grants-1979_05