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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2121486Generated: November 4, 2026

Sodium borohydride → HCID 10193644, compound

https://huagongshe.com/reaction/2121486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 69997187HCID 69997187—
SolventMethanolHCID 887—
ProductHCID 10193644HCID 1019364419.9%

Reaction Steps

At room temperature, 0.2 g of sodium borohydride are added in small portions to 0.4 g of (8R, 9R)-8-hydroxy-6-methoxymethyl-2,3-dimethyl-9-phenyl-7,8,9,10-tetrahydroimidazo[1 ,2-h][1,7]naphthyridin-7-one, dissolved in 20 ml of methanol, and the mixture is stirred at room temperature for 2 hours. The solvent is then removed under reduced pressure and the residue is admixed with water and extracted 3 times with methylene chloride. The organic phases are combined and concentrated to dryness in vacuo. Purification on silica gel (mobile phase: methylene chloride/methanol=100/3) gives 80 mg of the title compound [Rf=0.54 (methylene chloride/methanol=13/1)] of melting point 182-3° C. (decomp.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06696461B2
Source datasetuspto-grants-2004_02
ORD IDord-cbf384580a784ea88be747e6a0ff54cc
Source noteuspto-grants-2004_02