HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonium Chloride → 1-(3-Phenyl-3H-imidazo[4,5-c]pyridin-2-yl)ethanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 1-(3-Phenyl-3H-imidazo[4,5-c]pyridin-2-yl)ethanone | HCID 68157793 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(3-Phenyl-3H-imidazo[4,5-c]pyridin-2-yl)ethanol | HCID 68157413 | 87% |
Reaction Steps
Sodium borohydride (0.27 g, 7.17 mmol) was added to a stirred suspension of 1-(3-phenyl-3H-imidazo[4,5-c]pyridin-2-yl)ethanone (0.85 g, 3.58 mmol) in methanol (20 mL) at 0° C. under nitrogen. The reaction mixture was stirred for 15 minutes then poured into saturated aqueous ammonium chloride solution and extracted with EtOAc (3×50 mL). The combined EtOAc extracts were washed with water, dried (Na2SO4) and concentrated in vacuo to give the title compound as a white solid (0.74 g, 87%). LCMS (method H): Rt 1.76 min, [M+H]+ 240.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08653089B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-91ed4a81a9364729b0f502ec606fda43 |
| Source note | uspto-grants-2014_02 |