HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1984977Generated: November 3, 2026
Sodium borohydride → 2'-Hydroxymethyl-biphenyl-4-carboxylic acid quinolin-7-ylamide
https://huagongshe.com/reaction/1984977
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 2'-Formyl-biphenyl-4-carboxylic acid quinolin-7-ylamide | HCID 11187278 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2'-Hydroxymethyl-biphenyl-4-carboxylic acid quinolin-7-ylamide | HCID 11772611 | — |
Reaction Steps
To a solution of 2′-formyl-biphenyl-4-carboxylic acid quinolin-7-ylamide, Example 28, (90 mg, 0.25 mmol) in MeOH (2 mL) was added sodium borohydride (20 mg, 0.51 mmol) and the mixture was stirred for 10 min at 0° C. The reaction mixture was diluted with EtOAc (50 mL) and washed with satd NH4Cl (5 mL). The EtOAc layer was separated, washed with brine, dried over MgSO4, and filtered. The filtrate was evaporated in vacuo and the residue was purified by silica gel column chromatography (gradient, 40 to 90% EtOAc/hexane) to provide the title compound as a yellow amorphous solid. MS (ESI, pos. ion.) m/z: 355 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07544803B2 |
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| Source dataset | uspto-grants-2009_06 |
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| ORD ID | ord-09922cbba4d34db992f2a2c23f733b15 |
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| Source note | uspto-grants-2009_06 |
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