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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1596798Generated: October 30, 2026

Ethanol → 2-Imino-5-[4-[2-(5-methyl-2-phenyl-oxazole-4-yl)-ethoxy]-benzothiophene-7-yl]-methyl-thiazolidine-4-one

https://huagongshe.com/reaction/1596798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantSodium AcetateHCID 517045—
ReactantThioureaHCID 2723790—
Reactant5-Methyl-4-[2-(7-amino-benzothiophene-4-yloxy)-ethyl]-2-phenyl-oxazoleHCID 15485665—
Product2-Imino-5-[4-[2-(5-methyl-2-phenyl-oxazole-4-yl)-ethoxy]-benzothiophene-7-yl]-methyl-thiazolidine-4-oneHCID 18402252—

Reaction Conditions

Temperature2 °C

Reaction Steps

190 g (0.380 mol) of 5-methyl-4-[2-(7-amino-benzothiophene-4-yloxy)-ethyl]-2-phenyl-oxazole were suspended in 2.85 1 of ethanol. 31.6 g (0.415 mol) of thiourea and 34.8 g of sodium acetate were added. After boiling for about 18 hours (reflux) the reaction mixture was cooled to 0 to 4° C. and stirred for 1.5 hours at this temperature. The precipitate was filtered with suction and washed twice with 250 mnl cold ethanol. 1.91 of water was added to the residue, the mixture was stirred for 10 minutes and the precipitate was filtered with suction and dried for 24 hours at 80° C. (vacuum).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06291685B1
Source datasetuspto-grants-2001_09
ORD IDord-4338e03645c048cc864b9c1b7be042f3
Source noteuspto-grants-2001_09