HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 885059Generated: October 31, 2026
7-Chloro-4-methoxy-1H-pyrrolo[2,3-c]pyridine → 1-(4-methoxy-1H-pyrrolo[2,3-c]pyridin-7-yl)-1H-1,2,4-triazole-3-carbonitrile
https://huagongshe.com/reaction/885059
Participants
| Role | Name | HCID | Charge |
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| Reactant | 7-Chloro-4-methoxy-1H-pyrrolo[2,3-c]pyridine | HCID 15987013 | — |
| Reactant | HCID 178510603 | HCID 178510603 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 1-(4-methoxy-1H-pyrrolo[2,3-c]pyridin-7-yl)-1H-1,2,4-triazole-3-carbonitrile | HCID 58026037 | 38% |
Reaction Steps
7-Chloro-4-methoxy-1H-pyrrolo[2,3-c]pyridine (4 g, 21.90 mmol), 1H-1,2,4-triazole-3-carbonitrile (6.18 g, 65.7 mmol) and copper (I) iodide (1.252 g, 6.57 mmol) were combined in pyridine (6 mL) in a sealed tube. The mixture was heated to 150° C. for 6 hrs. After cooling to room temperature, the mixture was diluted with EtOAc (3000 mL), washed with 5% NaHCO3 (100 mL), brine (100 mL) and concentrated. The residue was purified by silica gel column using 30% EtOAc in hexanes mixture to give 1-(4-methoxy-1H-pyrrolo[2,3-c]pyridin-7-yl)-1H-1,2,4-triazole-3-carbonitrile (2 g, 8.33 mmol, 38.0% yield). LCMS: m/z 241.1 (M+H), 1.67 min (method 8).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08242124B2 |
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| Source dataset | uspto-grants-2012_08 |
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| ORD ID | ord-223b657cd7f14d8ba11728e870fcc519 |
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| Source note | uspto-grants-2012_08 |
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