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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2412456Generated: November 3, 2026

Ethyl bromopyruvate → HCID 178470110, compound

https://huagongshe.com/reaction/2412456

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromopyruvateHCID 66144—
ReactantHCID 178513045HCID 178513045—
SolventEthanolHCID 702—
ProductHCID 178470110HCID 17847011084.1%

Reaction Steps

A suspension of guanylthiourea (2.36 g) and ethyl 3-bromopyruvate (4.8 g) in dry ethanol (50 ml) is refluxed under stirring for 2.5 hours. The reaction mixture is concentrated in vacuum to dryness, and the residue is dissolved in water (about 100 ml). The aqueous solution is washed with ethyl acetate and made alkaline with 5% sodium hydrogencarbonate solution. The precipitated crystals are filtered, washed with water and dried to give 2-guanidino-4-ethoxycarbonylthiazole (3.6 g) as crystals. The yield is 84%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04492794
Source datasetuspto-grants-1985_01
ORD IDord-7d65f74aa0b54ad3a7ac5a88b14fab1d
Source noteuspto-grants-1985_01