HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 30062Generated: October 30, 2026
Boron Trichloride → HCID 69211615, compound
https://huagongshe.com/reaction/30062
Participants
| Role | Name | HCID | Charge |
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| Reactant | Boron Trichloride | HCID 25135 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-benzyloxymethyl-7-methoxy-N-[1-(naphthalen-2-ylmethyl)piperidin-4-yl]phthalazin-1-amine | HCID 69212668 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69211615 | HCID 69211615 | 58.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07423030B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-191cd4dbd06c46a684baff88706f32a3 |
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| Source note | uspto-grants-2008_09 |
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