Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 466015Generated: October 29, 2026

1,3,4-Thiadiazole, 2-amino-5-methyl- → HCID 15158115, compound

https://huagongshe.com/reaction/466015

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3,4-Thiadiazole, 2-amino-5-methyl-HCID 66949—
Reactant3-(2-Bromoacetyl)-2-phenylpyrazolo[1,5-a]pyridineHCID 15158181—
Solvent1-ButanolHCID 263—
ProductHCID 15158115HCID 1515811554.2%

Reaction Steps

A mixture of 3-(2-bromoacetyl)-2-phenylpyrazolo[1,5-a]pyridine (1.87 g), 2-amino-5-methyl-1,3,4-thiadiazole (0.68 g) and 1-butanol (19 ml) was refluxed for 5 hours and 20 minutes. The reaction mixture was evaporated in vacuo and the residue was taken up methylene chloride (40 ml). The methylene chloride solution was washed with an aqueous solution of potassium carbonate and dried over magnesium sulfate. The solvent was removed and the residue was subjected to chromatography on silica gel (25 g) with chloroform as an eluent. The fractions containing the objective compound were combined and evaporated in vacuo to give 3-(2-methylimidazo[2,1-b][1,3,4]thiadiazol-6-yl)-2-phenylpyrazolo[1,5-a]pyridine (1.06 g), which was recrystallized from acetone gave crystals (0.69 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05155114
Source datasetuspto-grants-1992_10
ORD IDord-7d73967641bf41eba31078a1b0c1ba42
Source noteuspto-grants-1992_10