Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714775Generated: October 30, 2026

Sodium borohydride → HCID 23155899, compound

https://huagongshe.com/reaction/1714775

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 23155961HCID 23155961—
SolventMethanolHCID 887—
ProductHCID 23155899HCID 2315589961.1%

Reaction Steps

To 10 ml of methanol, 300 mg of sodium borohydride was added and into this mixture, a solution of 145 mg of 6,6-ethylenedioxy-3-isopropylideneamino-2-[4-(4-quinolin-2-ylpiperazin-1-yl)butyl]-5,6,7,8-tetrahydro-3H-quinazolin-4-one as synthesized in Example 4-67 in 10 ml of methanol was dropped under cooling with ice. Raising the temperature to room temperature, the reaction mixture was stirred for an hour. Distilling the system under reduced pressure, water was added to the distillation residue, extracted with methylene chloride, washed with water, dried over anhydrous magnesium sulfate and the solvent was distilled off under reduced pressure. The residue was purified on silica gel column chromatography (methanol:methylene chloride=2:23) to provide 89 mg (61%) of 6,6-ethylenedioxy-3-isopropylamino-2-[4-(4-quinolin-2-ylpiperazin-1-yl)butyl]-5,6,7,8-tetrahydro-3H-quinazolin-4-one.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07799775B2
Source datasetuspto-grants-2010_09
ORD IDord-58697b6245034250ba62f0491dbe5b6a
Source noteuspto-grants-2010_09