HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1714775Generated: October 30, 2026
Sodium borohydride → HCID 23155899, compound
https://huagongshe.com/reaction/1714775
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 23155961 | HCID 23155961 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 23155899 | HCID 23155899 | 61.1% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07799775B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-58697b6245034250ba62f0491dbe5b6a |
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| Source note | uspto-grants-2010_09 |
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