HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium borohydride → HCID 71280581, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 71280624 | HCID 71280624 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 71280581 | HCID 71280581 | — |
Reaction Steps
To a stirring solution of N-(2-methyl-5-(5-(6-oxospiro[3.3]heptan-2-yl)-1,2,4-oxadiazol-3-yl)phenyl)imidazo[1,2-a]pyridine-3-carboxamide (F76) (100 mg, 0.23 mmol) in anhydrous methanol (1 mL) was added sodium borohydride (10.6 mg, 0.28 mmol). The reaction mixture was stirred at room temperature for 12 hours. The reaction was quenched with water and the solvent was concentrated. Purification by silica gel using 10% MeOH in dichloromethane afforded N-(5-(5-(6-hydroxyspiro[3.3]heptan-2-yl)-1,2,4-oxadiazol-3-yl)-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamide (F100). MS m/z 430.1 (M+1)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09199981B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-a769035ebfa9456c98cb7afc0a536eac |
| Source note | uspto-grants-2015_12 |