HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Fluoro-6-methoxybenzaldehyde → HCID 67517547, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Fluoro-6-methoxybenzaldehyde | HCID 2737357 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | HCID 67518282 | HCID 67518282 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 67517547 | HCID 67517547 | 40.3% |
Reaction Steps
Added 2-Fluoro-6-methoxy benzaldehyde (69 mg, 0.44 mmol) to a mixture of (R)-5-(5-(piperidin-3-yl)-1H-1,2,4-triazol-3-yl)-3-(pyridin-4-yl)-1H-indazole (96 mg, 0.277 mmol) and sodium triacetoxy borohydride (176 mg, 0.833 mmol) in MeOH (8 ml) at room temperature. After stirred for 30 minutes, the solvent was evaporated. Diluted with EtOAc (150 ml), washed with H2O (50 ml), dried (Na2SO4) and concentrated. Crude product was purified on silica gel eluting with 5% v/v MeOH/CH2Cl2 to yield (R)-5-(5-(1-(2-fluoro-6-methoxybenzyl)piperidin-3-yl)-1H-1,2,4-triazol-3-yl)-3-(pyridin-4-yl)-1H-indazole as a white solid (54 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08999966B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-ceef6e827a6840d2981057598614ea1b |
| Source note | uspto-grants-2015_04 |