HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium cyanoborohydride → HCID 19029368, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | 4-Phenylpiperidin-4-ol hydrochloride | HCID 18614383 | — |
| Reactant | HCID 19029354 | HCID 19029354 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | HCID 19029368 | HCID 19029368 | 70.9% |
Reaction Steps
2-[3-(3,4-dichlorophenyl)-1,5-dioxopentyl]-1,2,3,4-tetrahydroisoquinoline (800 mg), in MeOH/THF (1:1, 20 mL) was treated sequentially with molecular sieves 3A (900 mg), 4-phenyl-4-hydroxypiperidine HCl (900 mg) and NaBH3CN (130 mg). The resulting mixture was stirred at room temperature for 18 hours. The reaction mixture was with quenched with water (20 mL) and diluted with CH2Cl2 (50 mL). The organic layer was separated and the aqueous layer extracted with CH2Cl2 (3×50 mL) The combined organic layers were dried over MgSO4, filtered and concentrated under reduced pressure to give the crude oil. Silica gel chromatography eluting with 1-2% MeOH/CH2Cl2 gave the title compound (810 mg). Mass spectrum (FAB): 537.2075.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05654316 |
| Source dataset | uspto-grants-1997_08 |
| ORD ID | ord-e3a594622c8f4f96aa5bc85caf03a9b8 |
| Source note | uspto-grants-1997_08 |