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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373222Generated: October 31, 2026

Sodium borohydride → HCID 69185447, compound

https://huagongshe.com/reaction/2373222

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86602407HCID 86602407—
CatalystDichloronickel;hexahydrateHCID 11791229—
SolventMethanolHCID 887—
SolventWaterHCID 962—
ProductHCID 69185447HCID 6918544725.4%

Reaction Conditions

Temperature-10 °C

Reaction Steps

To a solution of ethyl (2E)-3-[4-(5-bromo-3-pyridyl)-1-ethyl-6-methyl-1H-pyrazolo[3,4-b]pyridin-5-yl]acrylate (47 mg) in MeOH (2 ml) was added nickel chloride hexahydrate (7.26 mg) and sodium borohydride (10.7 mg) at −10° C. and the mixture was stirred at −10° C. for 15 minutes. The reaction mixture was diluted with water and extracted with EtOAc. The organic layer was washed with water and dried over anhydrous MgSO4 and concentrated in vacuo. The residue was purified by preparative thin layer chromatography eluting with a mixture of EtOAc and n-hexane (1:1.5) to give ethyl 3-[4-(5-bromo-3-pyridyl)-1-ethyl-6-methyl-1H-pyrazolo[3,4-b]pyridin-5-yl]propanoate (12 mg) as a light yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459451B2
Source datasetuspto-grants-2008_12
ORD IDord-b011a562759b47b7b73983cc49acf1dd
Source noteuspto-grants-2008_12