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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506237Generated: October 30, 2026

Sodium Hydroxide → HCID 86726639, compound

https://huagongshe.com/reaction/1506237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant4-CyanobenzaldehydeHCID 66042—
ReactantBorane;2-methylpyridineHCID 16217944—
ReactantHCID 86726638HCID 86726638—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
ProductHCID 86726639HCID 8672663940%

Reaction Steps

1-(Piperidin-4-yl)-7-{[2-(trimethylsilyl)ethoxy]methyl}-1H-pyrrolo[3′,2′:5,6]pyrido[4,3-d]pyrimidine-2,4(3H,7H)-dione hydrochloride (50 mg, 0.111 mmol) and 4-cyanobenzaldehyde (29 mg, 0.22 mmol) in a mixture of methanol (2 ml) and acetic acid (0.2 mL) were stirred with 2-picoline borane (50 mg, 0.47 mmol) at room temperature for 2 days. After addition of 1 M aqueous sodium hydroxide, the reaction mixture was extracted with a mixture of ethyl acetate and 2-propanol, and the organic layer was dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography (chloroform/methanol=10/1 (v/v)) to give the title compound as a colorless solid (23.4 mg, yield 40%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216999B2
Source datasetuspto-grants-2015_12
ORD IDord-7c4bf4ede0ae43f59c12a9490a939df3
Source noteuspto-grants-2015_12