참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1,2-Dichloroethane | HCID 11 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 2-Mepp | HCID 91965 | — |
| 반응물 | 2-(2,4-Dimethoxyphenyl)acetic acid | HCID 350555 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 1-(2,4-Dimethoxyphenylacetyl)-4-(2-methylphenyl)piperazine | HCID 8297091 | — |
반응 단계
1-(2-methylphenyl)piperazine (.087 g, 0.41 mmol) and 2,4-dimethoxyphenylacetic acid (0.096 g, 0.49 mmol) were dissolved in 20 DMF (5 ml) and treated with EDC (0.091 g, 0.47 mmol) and HBT (0.071 g, 0.52 mmol). Triethylamine was added to the stirred mixture to bring the pH (moistened E. Merck colorpHast indicator) to ca. 9. The mixture was stirred at ambient temperature for 18 hours, then concentrated in vacuo. The residue was taken up in ethyl acetate, and the ethyl acetate layer was washed with saturated aqueous sodium bicarbonate and brine, dried over sodium sulfate, filtered, and the filtrate was concentrated to dryness in vacuo. The residue was chromatographed on silica gel eluted with 1.5% methanol in methylene chloride. The combined product fractions were evaporated to dryness in vacuo to give the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05756504 |
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| 출처 데이터셋 | uspto-grants-1998_05 |
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| ORD ID | ord-6c0f53a3127d4a04baf5e948c80f9ef1 |
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| 출처 메모 | uspto-grants-1998_05 |
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