HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 717556Generated: October 30, 2026
HCID 178512052, compound → 7-Chloro-2-(5-cyclopropylpyridin-3-yl)-[1,2,4]triazolo[1,5-a]pyridine
https://huagongshe.com/reaction/717556
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 178512052 | HCID 178512052 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 7-Chloro-2-(5-cyclopropylpyridin-3-yl)-[1,2,4]triazolo[1,5-a]pyridine | HCID 86729656 | — |
Reaction Steps
Lead tetra acetate (0.684 g, 0.0015 mol) was added to a solution of N-(4-chloropyridin-2-yl)-5-cyclopropylnicotinimidamide (42-1; 0.280 g, 0.001 mol) in toluene (30 mL) in a 40 mL microwave vial at RT. The reaction mixture was heated to 150° C. for 2 h under microwave irradiation. It was cooled to RT then diluted with water (50 mL) and extracted with ethyl acetate (2×50 mL). The combined organic layer was dried over sodium sulphate and concentrated under vacuum to afford the crude product, which was purified by silica gel column chromatography to afford the title compound. 1H NMR (400 MHz, DMSO) δ 9.08-9.02 (t, J=7.2 Hz, 2H), 8.52 (s, 1H), 8.10-8.05 (d, J=18.4 Hz, 2H), 7.32-7.31 (d, J=6.8 Hz, 1H), 2.08 (s, 1H), 1.07-1.05 (d, J=10.4 Hz, 2H), 0.82-0.81 (d, J=4.4 Hz, 2H). MS (M+1): 271.7.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193724B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-e527f1541bc045ce92dff6f57faa59dd |
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| Source note | uspto-grants-2015_11 |
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