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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1373951Generated: November 3, 2026

Sodium borohydride → HCID 21075799, compound

https://huagongshe.com/reaction/1373951

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 21075800HCID 21075800—
SolventMethanolHCID 887—
ProductHCID 21075799HCID 2107579988.1%

Reaction Steps

A solution of N-(7-bromo-2-propyl-1H-imidazo[4,5-c]quinolin-1-yl)isopropylideneamine (18.4 g, 53.3 mmol) in 100 mL of methanol was placed under an atmosphere of nitrogen and cooled in an ice water bath. The solution was treated with sodium borohydride (2.32 g, 61.3 mmol) over 30 min. The reaction mixture was allowed to slowly come to ambient temperature. After 1.5 h, the reaction was quenched by the addition of 25 mL of saturated NH4Cl solution. The reaction mixture was concentrated under reduced pressure to remove the methanol. The residue was partitioned between chloroform (150 mL) and 10% Na2CO3 solution (35 mL), and the phases were separated. The organic portion was washed with another portion of 10% Na2CO3 solution (35 mL), water (35 mL) and brine (35 mL). The organic portion was dried over Na2SO4, filtered and concentrated under reduced pressure to yield a brown foam. The foam was purified by chromatography (SiO2, 97:3 CHCl3:MeOH gradient to 9:1) to give 16.3 g of N-(7-bromo-2-propyl-1H-imidazo[4,5-c]quinolin-1-yl)isopropylamine as a dark tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07163947B2
Source datasetuspto-grants-2007_01
ORD IDord-2d6dedb274154293a4d53576cf7bf754
Source noteuspto-grants-2007_01