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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966818Generated: November 2, 2026

Sodium borohydride → HCID 25073835, compound

https://huagongshe.com/reaction/1966818

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 66733157HCID 66733157—
CatalystMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 25073835HCID 25073835—

Reaction Steps

Sodium borohydride (14 mg, 0.00036 mole) was added to methyl 3-[4-(cyclohexylamino)-1-ethyl-1H-pyrazolo[3,4-b]pyridin-5-yl]-5-(2-methoxy-2-oxoethyl)-4,5-dihydroisoxazole-5-carboxylate (80 mg, 0.00018 mole) (example 10) in tetrahydrofuran (5 ml). Methanol (2 drops) was added and the reaction mixture was stirred at room temperature overnight. It was quenched with saturated ammonium chloride solution, diluted with ethyl acetate and extracted with brine. The organic layer was dried over anhydrous sodium sulphate and concentrated in vacuo. The crude product was purified by column chromatography.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420666B2
Source datasetuspto-grants-2013_04
ORD IDord-7ce56d18ecd24a0ca6f9ea9d4388cb35
Source noteuspto-grants-2013_04