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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373914Generated: November 1, 2026

Sodium borohydride → HCID 21075790, compound

https://huagongshe.com/reaction/1373914

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 69177440HCID 69177440—
SolventMethanolHCID 887—
ProductHCID 21075790HCID 2107579090.8%

Reaction Steps

A solution of N-(2-ethoxymethyl-1H-imidazo[4,5-c]quinolin-1-yl)(furan-2-ylmethylene)amine (1.86 g, 5.81 mmol) in 20 mL of methanol was treated with NaBH4 (0.659 g, 17.4 mmol) and stirred under an atmosphere of nitrogen. After 18 h the reaction was quenched by addition of 20 mL of water. The reaction mixture was concentrated under reduced pressure and dissolved in CHCl3. The organic portion was washed with 2% Na2CO3 solution, water and brine, dried over Na2SO4, filtered and concentrated under reduced pressure to yield N-(2-ethoxymethyl-1H-imidazo[4,5-c]quinolin-1-yl)(furan-2-ylmethyl)amine (1.70 g) as a thick orange syrup.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07163947B2
Source datasetuspto-grants-2007_01
ORD IDord-e00c4c06eead4bacba633652b4748d8b
Source noteuspto-grants-2007_01