HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 234117Generated: October 25, 2026
2-[4-(5-Bromo-2-methoxybenzyl)-1-piperazinyl]pyrimidine → 4-Phenyl-2-[(4-(2-pyrimidinyl)-piperazinyl)methyl]anisole
https://huagongshe.com/reaction/234117
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-[4-(5-Bromo-2-methoxybenzyl)-1-piperazinyl]pyrimidine | HCID 1240303 | — |
| Reactant | HCID 178418255 | HCID 178418255 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-Phenyl-2-[(4-(2-pyrimidinyl)-piperazinyl)methyl]anisole | HCID 9845721 | — |
Reaction Steps
A solution of 182 mg 2-[(4-(2-pyrimidinyl)-piperazinyl)methyl]-4- bromoanisole in 1 mL of tetrahydrofuran heated to 60° C. and 6 mg of Pd(PPh3)4 was added. To this mixture 0.5 mL of a 1M solution of phenylmagnesium bromide in tetrahydrofuran was added dropwise. The reaction mixture was heated at relux temperature under nitrogen for 1 hr, cooled to room temperature and the solvent removed by evaporation under reduced pressure to yield 4-phenyl-2-[(4-(2-pyrimidinyl)-piperazinyl)methyl]anisole which was purified by chromatography on silica gel using 5% methanol in dichloromethane as eluent. Evaporation of the solvent yielded 140 mg of a solid which was treated with ethyl acetate-HCl to give 50 mg of 4-phenyl-2-[(4-(2-pyrimidinyl)piperazinyl)methyl]anisole dihydrochloride (Compound 1 ), mp 205°-207° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05594141 |
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| Source dataset | uspto-grants-1997_01 |
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| ORD ID | ord-4919be748fa34c228f15b152956edf7a |
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| Source note | uspto-grants-1997_01 |
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