HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,6-dinitro-2H-indazole → 3-Methoxy-6-nitro-1H-indazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,6-dinitro-2H-indazole | HCID 330840 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 3-Methoxy-6-nitro-1H-indazole | HCID 68443492 | — |
Reaction Steps
To a solution of 2,6-dinitro-2H-indazole(1 mmol) (prepared by nitration of 6-nitroindazole; Wrzeciono, et al., E. Pharmazie, 1980, 35, 593-596) in dry THF (4 mL) at 0° C., solid sodium methoxide (4 mmol) was added in portions. The reaction mixture was allowed to warm to room temperature and stirred for 12 h. The contents were diluted with ethyl acetate (20 mL), washed with water (2×10 mL) and brine (10 mL) and dried over anhydrous sodium sulfate. The solvent was removed in vacuo to yield 3-methoxy-6-nitro-1H-indazole as a brown solid, which was reduced to 3-methoxy-1H-indazol-6-ylamine by hydrogenation following general procedure F.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07820821B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-16960ba570f141ad91e48d04b7e1d804 |
| Source note | uspto-grants-2010_10 |