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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3,4-Thiadiazole, 2-amino-5-methyl- | HCID 66949 | — |
| Reactant | 3-(2-Bromoacetyl)-2-phenylpyrazolo[1,5-a]pyridine | HCID 15158181 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 15158115 | HCID 15158115 | 54.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05155114 |
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| Source dataset | uspto-grants-1992_10 |
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| ORD ID | ord-7d73967641bf41eba31078a1b0c1ba42 |
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| Source note | uspto-grants-1992_10 |
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