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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497938Generated: October 30, 2026

Sodium borohydride → HCID 71280581, compound

https://huagongshe.com/reaction/1497938

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 71280624HCID 71280624—
SolventMethanolHCID 887—
ProductHCID 71280581HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199981B2
Source datasetuspto-grants-2015_12
ORD IDord-a769035ebfa9456c98cb7afc0a536eac
Source noteuspto-grants-2015_12