참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Tributylamine | HCID 7622 | — |
| 반응물 | 3,3-Diethoxy-1-propene | HCID 62477 | — |
| 반응물 | 3-(5-Methyl-2-tetrazol-1-yl-phenyl)-propionic acid | HCID 66938857 | — |
| 촉매 | Tetrabutylammonium Chloride | HCID 70681 | — |
| 촉매 | palladium(II) acetate | HCID 167845 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 3-(5-Methyl-2-tetrazol-1-yl-phenyl)-propionic acid ethyl ester | HCID 66938341 | 66.8% |
반응 단계
3-(5-Methyl-2-tetrazol-1-yl-phenyl)-propionic acid: To a mixture of 117A (956 mg, 4.00 mmol), 3,3-diethoxyprop-1-ene (1562 mg, 12.00 mmol), and Bu4NCl (1110 mg, 4.00 mmol) in DMF (22 mL) was added Bu3N (1480 mg, 8.00 mmol). To this mixture under N2 was added Pd(OAc)2 (26.9 mg, 0.12 mmol). The resulting mixture was stirred at 90° C. for 1.5 h, then cooled to rt and quenched with 2N HCl (10 mL). The resulting mixture was stirred for 20 min, then evaporated. The mixture was diluted with EtOAc, washed with water and brine, dried over MgSO4, and purified by flash chromatography to provide 3-(5-Methyl-2-tetrazol-1-yl-phenyl)-propionic acid ethyl ester (695 mg, 66.8%). LCMS m/z 261.2 (M+H)+. To a solution of this intermediate (690 mg, 2.65 mmol), in THF (10 mL) was added 2N LiOH (10 mL). The resulting mixture was stirred at rt for 3 h, then acidified to pH 3-4 with 2N HCl at 0° C. The mixture was concentrated and extracted with EtOAc (5×20 mL). The combined organic layers were washed with brine, dried over MgSO4, and purified by prep. HPLC to give 117B (567 mg, 92%). LCMS m/z 233.2 (M+H)+.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08604056B2 |
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| 출처 데이터셋 | uspto-grants-2013_12 |
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| ORD ID | ord-2793b045dbb04492a06312c17e14e888 |
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| 출처 메모 | uspto-grants-2013_12 |
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