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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1193438Generated: November 2, 2026

Ethanol → HCID 178513114, compound

https://huagongshe.com/reaction/1193438

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 numberUS04810282
Source datasetuspto-grants-1989_03
ORD IDord-b3da985d89094800a34e2713ad013835
Source noteuspto-grants-1989_03