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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30062Generated: October 30, 2026

Boron Trichloride → HCID 69211615, compound

https://huagongshe.com/reaction/30062

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBoron TrichlorideHCID 25135—
ReactantSodium BicarbonateHCID 516892—
Reactant4-benzyloxymethyl-7-methoxy-N-[1-(naphthalen-2-ylmethyl)piperidin-4-yl]phthalazin-1-amineHCID 69212668—
SolventDichloromethaneHCID 6344—
ProductHCID 69211615HCID 6921161558.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 120 mg of 4-benzyloxymethyl-7-methoxy-N-[1-(naphthalen-2-ylmethyl)piperidin-4-yl]phthalazin-1-amine in 4 mL of dichloromethane is stirred under nitrogen at 0° C., followed by dropwise addition of 2.3 mL of a molar solution of boron trichloride in dichloromethane. The reaction medium is stirred for 1 hour at 0° C. and then for 30 minutes at room temperature. It is hydrolysed with aqueous sodium bicarbonate solution and extracted with dichloromethane. The organic phase is washed with water, dried over anhydrous sodium sulfate, filtered and evaporated under reduced pressure. The residue is purified on a column of silica (eluent: 100/0 to 85/15 v/v dichloromethane/methanol). 58 mg of product are obtained in the form of a beige-coloured powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07423030B2
Source datasetuspto-grants-2008_09
ORD IDord-191cd4dbd06c46a684baff88706f32a3
Source noteuspto-grants-2008_09