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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2379827Generated: November 1, 2026

N-(2-amino-2-thioxoethyl)acetamide → HCID 18956300, compound

https://huagongshe.com/reaction/2379827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-amino-2-thioxoethyl)acetamideHCID 4435531—
ReactantHCID 18956304HCID 18956304—
SolventEthanolHCID 702—
ProductHCID 18956300HCID 1895630049.7%

Reaction Steps

A suspension of 2-amino-4-bromoacetylthiazole hydrobromide (14.0 g) and N-[(thiocarbamoyl)methyl]-acetamide (6.1 g) in ethanol (300 ml) was stirred at room temperature for 24 hours. The insoluble material was removed by filtration. The solvent was removed under reduced pressure. The residue was suspended in water (300 ml). The mixture was alkalized to pH 10 with a saturated aqueous potassium carbonate solution and then was extracted with a mixture of ethyl acetate (500 ml) and tetrahydrofuran (100 ml). The extract was dried over magnesium sulfate and then was evaporated to afford 4-(2-acetylaminomethylthiazol-4-yl)-2-aminothiazole (5.83 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05364871
Source datasetuspto-grants-1994_11
ORD IDord-0577b30e88e84864981085cef14fde49
Source noteuspto-grants-1994_11