Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 364836Generated: November 2, 2026

Ethanol → HCID 178513114, compound

https://huagongshe.com/reaction/364836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
ReactantGuanidineHCID 3520—
ReactantHCID 178526588HCID 178526588—
SolventTetrahydrofuranHCID 8028—
ProductHCID 178513114HCID 178513114—

Reaction Steps

The reactions of Equation 57 above can be run by methods known in the art. Thus, in reaction 57a, a 2-nitrothiobenzoate of Formula (LXXV) is reacted with guanidine in a solvent such as ethanol or tetrahydrofuran at 0° to about 30° C. for 2 to 120 hours to form a 2-nitrothiobenzoylguanidine of Formula (LXXVI), according to the teachings of J. Goerdeler and A. Fincke, Chem. Ber., 89, 1033 (1956). In reaction 57b, LXXVI is cyclized by reaction with bromine in methanol at 0° to 60° C. for 0.5 to 3 hours to form a 3-amino-5-(2-nitrophenyl)-1,2,4-thiadiazole of Formula (LXXVII), according to the teachings of ibid. In reaction 57c, LXXVII is reacted with sodium nitrite in hydrochloric acid or hydrobromic acid, in the presence of copper powder, at -10° to 60° C. for 0.5 to 5 hours to form Xq' via Sandmeyer reaction, according to the teachings of F. Kurzer and S. Taylor, J. Chem. Soc., 3234 (1960). And in the last reaction, Xq' is reacted with sodium methoxide, sodium ethoxide or sodium methylmercaptide in a solvent such as methanol, ethanol or tetrahydrofuran at reflux for 0.5 to 5 hours to form Xq", according to the teachings of ibid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04606755
Source datasetuspto-grants-1986_08
ORD IDord-0c94919ddc384a39807aa379a035270d
Source noteuspto-grants-1986_08