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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 67981Generated: October 29, 2026

Acetic Anhydride → HCID 178485063, compound

https://huagongshe.com/reaction/67981

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 178485064HCID 178485064—
SolventWaterHCID 962—
SolventPyridineHCID 1049—
ProductHCID 178485063HCID 178485063—

Reaction Steps

Acetic anhydride (0.39 g.) was added to a stirred suspension of 2-guanidino-4-[2-(2-cyano-3-methylguanidino)ethylthiomethyl]thiazole (1.10 g.) in pyridine (6 ml.) at room temperature. After stirring for two hours, the mixture was diluted with water (50 ml.), extracted with methylene chloride (3×30 ml.) and the combined extracts washed with water (100 ml.) and dried over magnesium sulphate. The solution was filtered and evaporated to dryness to leave a gum which was purified by column chromatography (silica column, eluted with ethyl acetate/ethanol/ammonia (s.g. 0.880) 6:1:1 v/v/v) to give 2-(2-acetylguanidino)-4-[2-(2-cyano-3-methylguanidino)ethylthiomethyl]thiazole as an amorphous solid. The n.m.r. spectrum in d6 dimethyl sulphoxide using tetramethylsilane as internal standard had the following resonances (δ): 2.1 (3H, singlet); 2.7 (5H, multiplet); 3.3 (multiplet, obscured by H2O); 3.7 (2H, singlet); 6.8 (1H, singlet); 7.0 (2H, broad multiplet); 9.0 (2H, very broad) and 10.7 (1H, broad).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04347370
Source datasetuspto-grants-1982_08
ORD IDord-3f179c1240ab4b01a65c4b499e72d9e6
Source noteuspto-grants-1982_08