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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1868466Generated: November 1, 2026

Sodium borohydride → HCID 86606997, compound

https://huagongshe.com/reaction/1868466

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86606995HCID 86606995—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86606997HCID 86606997110.8%

Reaction Steps

To a stirred solution of tert-butyl (2-acetyl-5-(2,4-dichlorophenyl)-7-methylimidazo[1,2-a]pyrimidin-6-yl)methylcarbamate (intermediate for Example 150, 5 mg, 0.01 mmol) in THF (2 mL) and H2O (0.3 mL) at room temperature was added NaBH4 (2 mg, 0.05 mmol). After 30 min, the reaction was concentrated under reduced pressure and diluted with EtOAc. The organic layer was washed with satd aq NH4Cl and brine prior to drying over MgSO4. Filtration, concentration under reduced pressure and purification by silica gel chromatography afforded crude tert-butyl (5-(2,4-dichlorophenyl)-2-(1-hydroxyethyl)-7-methylimidazo[1,2-a]pyrimidin-6-yl)methylcarbamate (5 mg, 100% crude yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07635699B2
Source datasetuspto-grants-2009_12
ORD IDord-1dc9de9efabb46f0b3ea420d35a104e6
Source noteuspto-grants-2009_12