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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1112055Generated: November 3, 2026

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

https://huagongshe.com/reaction/1112055

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-(5-Tert-butyl-1,3,4-thiadiazol-2-ylcarbamoylmethyl)-2-aminothiazoleHCID 21321148—
SolventPropionic anhydrideHCID 31263—
Product4-(5-Tert-butyl-1,3,4-thiadiazol-2-ylcarbamoylmethyl)-2-propionamidothiazoleHCID 2132116567.2%

Reaction Steps

A mixture of 4.8 g (0.016 mole) of 4-(5-tert-butyl-1,3,4-thiadiazol-2-ylcarbamoylmethyl)-2-aminothiazole dissolved 20 ml of propionic anhydride was heated for 1 hour at 90°. The reaction solution was cooled and the precipitate was collected. The crude solid was recrystallized from chloroform-hexane. There was obtained 1.9 g of product, m.p. 210°-12°. N.M.R. (CDCl3) ∂ 1.1-1.4 (CH3, triplet), 1.4 [C(CH3)3 ], 2.3-2.7 (CH2, quartet), 3.9 (CH2, singlet), 6.8 (hetero-aromatic).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04120690
Source datasetuspto-grants-1978_10
ORD IDord-4999d11f3850410e8c3a78f2d811abe0
Source noteuspto-grants-1978_10