HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → 6,11-DIHYDRO-11-(4-PIPERIDINYL)-5H-BENZO[5,6]CYCLOHEPTA[1,2-b]PYRIDINE
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | (1-Methylpiperidin-4-yl)[3-(2-phenylethyl)pyridin-2-yl]methanone | HCID 14885588 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6,11-DIHYDRO-11-(4-PIPERIDINYL)-5H-BENZO[5,6]CYCLOHEPTA[1,2-b]PYRIDINE | HCID 10684018 | 97.6% |
Reaction Steps
To a mixture of 5.0 g (16.2 mmole) of (1-methyl-4-piperidinyl) [3-(2-phenylethyl)-2-pyridinyl]methanone (which can be prepared in the same manner as described in Preparative Example 1, Steps A-D) in 70 mL of methanol was added portionwise 0.8 g (21.1 mmole) of sodium borohydride. The next day the solution was concentrated in vacuo to give a slurry which was dissolved in water and extracted with CHCl3. The combined organic portions were dried over MgSO4, filtered, and concentrated in vacuo to provide a liquid which was distilled (bp 190°-195° C. 1 mm Hg) to give 4.4 gms of the title compound as a viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05665726 |
| Source dataset | uspto-grants-1997_09 |
| ORD ID | ord-3ed45a8f3144400cb2f79868d3e8c6a7 |
| Source note | uspto-grants-1997_09 |