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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 622711Generated: October 26, 2026

Ethyl orthoformate → HCID 178482140, compound

https://huagongshe.com/reaction/622711

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl orthoformateHCID 31214—
Reactant1-(4-(3-Aminophenyl)thiazol-2-yl)guanidineHCID 178512611—
CatalystTrifluoroacetic acidHCID 6422—
ProductHCID 178482140HCID 178482140—

Reaction Conditions

Temperature0 °C

Reaction Steps

A mixture of 9.3 g (0.04 mole) of 3-(2-guanidino-4-thiazolyl)benzeneamine, 20 ml of triethylorthoformate, and 2 drops of trifluoroacetic acid is stirred at reflux for 5 hours after which it is concentrated in vacuo. The residue is dissolved in 20 ml of ethanol, the solution cooled to 0° C. and then treated with excess sodium borohydride. The mixture is allowed to warm to room temperature, then stirred at reflux for 4 hours. Upon concentration in vacuo the residue is partitioned between water and dichloromethane.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04772622
Source datasetuspto-grants-1988_09
ORD IDord-bf26f55371854a828c4f5bb935c679d5
Source noteuspto-grants-1988_09