HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 22614977, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 22615088 | HCID 22615088 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 22614977 | HCID 22614977 | 60.6% |
Reaction Steps
To a solution of (5-methyl-isoxazol-3-yl)-{3-methyl-4-[3-(methyl-pyridin-3-ylmethyl-amino)-propoxy]-benzofuran-2-ylmethylene}-amine (46 mg) in methanol (2 ml) was added sodium borohydride (20 mg) at room temperature. After 1 hour the mixture was concentrated in vacuo and purified by silica gel column chromatography developed by dichloromethane and methanol to give the titled compound as white solids (28 mg). ESI-MS: m/z 421 (MH+); 1H-NMR (CDCl3): δ 1.97-2.06 (2H, m), 2.25 (3H, s), 2.27 (3H, s), 2.28 (3H, s), 2.59 (2H, t, J=6.9 Hz), 3.52 (2H, s), 4.09 (2H, t, J=5.94 Hz), 4.41 (2H, s), 5.53 (1H, s), 6.58 (1H, d, J=7.6 Hz), 7.00 (1H, d, J=7.6 Hz), 7.05-7.15 (2H, m), 7.59-7.63 (1H, m), 8.39 (1H, dd, J=1.7 Hz, 4.9 Hz), 8.49 (1H, d, J=2.0 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06376491B1 |
| Source dataset | uspto-grants-2002_04 |
| ORD ID | ord-09fb89491dc94973bb87dbfd82e10d3a |
| Source note | uspto-grants-2002_04 |