HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 117668009, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 117668210 | HCID 117668210 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 117668009 | HCID 117668009 | 70.9% |
Reaction Steps
To a solution of ethyl 4-(5-amino-4-cyano-3-(4-phenoxyphenyl)-1H-pyrazol-1-yl)-1-benzylpiperidine-4-carboxylate (52 mg, 0.1 mmol) in MeOH (5 mL) was added NaBH4 (8 mg, 0.2 mmol). After 10 min, the reaction was quenched with water (5 mL) and extracted with EA (10 mL×3). The organic combined layers was dried over Na2SO4 and concentrated to give the crude product (34 mg, 70.9%) as an off-white solid. MS (ESI, m/e) [M+1]+ 480.0.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09447106B2 |
| Source dataset | uspto-grants-2016_09 |
| ORD ID | ord-84685ff8f0574948b44ff727fdf00f66 |
| Source note | uspto-grants-2016_09 |