HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 5-(1,2,4-triazol-4-yl)-1H-pyrrolo[2,3-c]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1,2-Hydrazinedicarboxaldehyde | HCID 12342 | — |
| Reactant | 1H-Pyrrolo(2,3-c)pyridin-5-amine | HCID 18975323 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-(1,2,4-triazol-4-yl)-1H-pyrrolo[2,3-c]pyridine | HCID 18975358 | 59.4% |
Reaction Steps
5-Amino-1H-pyrrolo[2,3-c]pyridine (2 g, 15 mmol), diformylhydrazine (1.32 g, 15 mmol) and dry DMF (1.5 mL) were heated at 170° C. under nitrogen for 4 hours. After cooling, ethyl acetate (10 mL) and water (10 mL) were added. The mixture was stirred vigorously for 15 min. The resulting precipitate was collected by filtration, and chromatographed on silica eluting with a gradient of 5 to 7 to 10% MeOH in DCM to give a yellow solid. This was triturated with ether to give the title compound (1.65 g, 59%) as a yellow/green crystalline solid. mp 254°-257° C. 1H NMR (360 MHz, d6 -DMSO) δ 6.63 (1H, d, J=3.1Hz), 7.79 (1H, d, J=3.0Hz), 7.99 (1H, s), 8.71 (1H, s), 9.21 (2H, s) and 11.89 (1H, br s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05807857 |
| Source dataset | uspto-grants-1998_09 |
| ORD ID | ord-a30dca9131174ecda669761d0526660f |
| Source note | uspto-grants-1998_09 |