HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → [3-(2-benzyl-7-trifluoromethyl-2H-indazol-3-yl)-phenyl]-methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 11675307 | HCID 11675307 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | [3-(2-benzyl-7-trifluoromethyl-2H-indazol-3-yl)-phenyl]-methanol | HCID 11703640 | — |
Reaction Steps
To a solution of 116 mg (0.305 mmol) of 3-[2-benzyl-7-(trifluoromethyl)-2H-indazol-3-yl]benzaldehyde (compound of Formula (I)), prepared in a same way as Example 1, in 2 ml of methanol, 23 mg (0.71 mmol) of NaBH4 was added at 0° C. The reaction mixture was stirred at this temperature for 1 hr. Saturated NH4Cl-solution and dichloromethane were added, and the phases were separated. The product was obtained after flash chromatographic purification using dichloromethane as eluant. Yield: 111 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07592363B2 |
| Source dataset | uspto-grants-2009_09 |
| ORD ID | ord-7de02031d20a4b919dc4c4c5421381bc |
| Source note | uspto-grants-2009_09 |