HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 215967Generated: October 29, 2026
Sodium borohydride → HCID 59176789, compound
https://huagongshe.com/reaction/215967
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | 3-[1-Naphthalen-1-yl-methylidene]-imidazo[1,2-a]pyridin-2-one | HCID 68699547 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 59176789 | HCID 59176789 | — |
Reaction Steps
To a suspension of 137 mg (3.7 mmol) of sodium borohydride in 15 mL of ethanol is added a solution of 500 mg (1.8 mmol) of 3-[1-naphthalen-1-yl-methylidene]-imidazo[1,2-a]pyridin-2-one in 50 mL of methanol, dropwise at −78° C. After stirring for 10 min at −78° C., the reaction mixture is quenched with saturated aqueous ammonium chloride solution at −78° C. The product is extracted with dichloromethane. The organic layer is dried over magnesium sulfate, filtered and concentrated in vacuo to give the desired compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08193214B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-22fb3b9ad2bc48f99a18ffab9dce5bc0 |
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| Source note | uspto-grants-2012_06 |
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