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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 703974Generated: October 30, 2026

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

https://huagongshe.com/reaction/703974

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 numberUS04985444
Source datasetuspto-grants-1991_01
ORD IDord-43ead621f30840d0957a1729b7b2743e
Source noteuspto-grants-1991_01