참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | Trimetazidine Dihydrochloride | HCID 83201 | — |
| 반응물 | 1,1'-(Chloromethylene)bis(4-fluorobenzene) | HCID 2723773 | — |
| 용매 | O-Xylene | HCID 7237 | — |
| 생성물 | Lomerizine Hydrochloride | HCID 122125 | 22.1% |
반응 단계
2.4 g (7.1 millimoles) of 2,3,4-trimethoxybenzylpiperazine dihydrochloride, 1.8 g (7.5 millimoles) of bis(4-fluorophenyl)methyl chloride [see J. Chem. Soc. Perkin II, 1051 (1977)] and 5.0 ml (36 millimoles) of triethylamine were heated under reflux for 9 hours in 80 ml of xylene. The reaction mixture was allowed to cool to room temprature, washed with water, and dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure. A mixture of 2 ml of conc. hydrochloric acid and 20 ml of ethanol was added to the resulting oily product, and the mixture was concentrated under reduced pressure. Ether was added, and the precipitated crystals were collected by filtration. Recrystallization of the crystals from ethanol-ether gave 0.85 g of 1-(2,3,4-trimethoxybenzyl)-4-[bis(4-fluorophenyl)methyl]piperazine dihydrochloride. The product showed the same property values as the compound obtained in Example 4.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04663325 |
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| 출처 데이터셋 | uspto-grants-1987_05 |
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| ORD ID | ord-a4e6364165b44ee2a74c0e6e9f851403 |
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| 출처 메모 | uspto-grants-1987_05 |
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