HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 86601776, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 68743987 | HCID 68743987 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86601776 | HCID 86601776 | — |
Reaction Steps
To a solution of tert-butyl 4-methyl-4-{3-methyl-4-[3-oxo-5-(trifluoromethyl)-2,3-dihydro-1H-inden-1-yl]piperazin-1-yl}piperidine-1-carboxylate (100 mg, 0.202 mmol) in ethanol (7 mL) was added sodium borohydride (57 mg, 1.5 mmol). The reaction mixture was stirred at room temperature for 2 h. The solvent was evaporated in vacuo, and the residue was quenched with 10 mL of 1 N aqueous NaOH solution and 10 mL of EtOAc. The organic phase was separated and the aqueous layer was extracted with EtOAc twice (2×15 mL). The combined extracts were washed with brine, dried over Na2SO4 and evaporated under reduced pressure to give the desired product which was directly used for the next step (93 mg, 92%). LC-MS [M+1]=498.4.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09067921B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-4b6609cb2b02471284aa92978cc13f6f |
| Source note | uspto-grants-2015_06 |