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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378601Generated: November 1, 2026

2-Methylthiazole-4-carbothioamide → HCID 22912398, compound

https://huagongshe.com/reaction/1378601

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Methylthiazole-4-carbothioamideHCID 2744365—
Reactant1-(4-Fluorophenyl)-2-(4-methylthiophenyl)-2-bromoethanoneHCID 54160532—
SolventEthanolHCID 702—
SolventAcetonitrileHCID 6342—
ProductHCID 22912398HCID 2291239849%

Reaction Steps

A solution of 1-(4-fluorophenyl)-2-(4-methylthiophenyl)-2-bromoethanone (9.69 g, 28.6 mmol) (Example 1, Step 3) and 2-methylthiazole-4-thiocarboxamide (3.90 g, 24.7 mmol) in 35 mL of acetonitrile and 20 mL of ethanol was heated to reflux for 1 hour. The solution was concentrated in vacuo and the residue was dissolved in ethyl acetate, washed with saturated aqueous NaHCO3, brine, dried over anhydrous MgSO4, filtered and concentrated in vacuo to give a yellow solid. The crude solid was purified by flash chromatography over silica gel eluting with 1:1 hexane:ethyl acetate. The appropriate fractions were combined and the solvent removed in vacuo to provide pure 4-(4-fluorophenyl)-5-(4-methylthiophenyl)-2-[2-(methyl)-4-thiazolyl]thiazole (4.79 g; 49%): mp 132.5°-135° C. 1H NMR (CDCl3) 300 MHz 7.89 (s, 1H), 7.55 (m, 2H), 7.25 (d, J=8.5Hz, 2H), 7.17 (d, J=8.5Hz, 2H), 7.01 (t, J=8.8Hz, 2H), 2.78 (s, 3H), 2.49 (s, 3H). 19F NMR (CDCl3) -113.80 (m). Mass spectrum M+H+ =399.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05668161
Source datasetuspto-grants-1997_09
ORD IDord-01fd508f80a244c2b7c190185e0fc4bd
Source noteuspto-grants-1997_09