関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | m-Anisoyl chloride | HCID 74374 | — |
| 反応物 | Ethyl 4-(2-aminophenyl)-4-oxobutanoate | HCID 21283602 | — |
| 溶媒 | Chloroform | HCID 6212 | — |
| 生成物 | Ethyl 2-(3-methoxyphenyl)-4-quinazolinepropionate | HCID 13769245 | — |
反応手順
3-Methoxybenzoyl chloride (2.81 cc) is added at 5° C. to ethyl 3-(2-aminobenzoyl)propionate (2.21 g) and triethylamine (4.2 cc) in chloroform (25 cc). The mixture is left for 1 hour at room temperature (approximately 20° C.), water (25 cc) is added and the mixture decanted. The organic phase is evaporated under reduced pressure and the residue taken up with ammonium acetate (17 g). The mixture is brought to 100° C. for 7 hours and the acetic acid formed is then evaporated off under reduced pressure. The residue is poured into water (100 cc) and the aqueous phase extracted with ethyl acetate (3×50 cc). The aqueous phase is dried over magnesium sulphate, filtered and evaporated to dryness under reduced pressure. The residual product is chromatographed in silica gel with a cyclohexane/ethyl acetate (1:1 by volume) mixture as eluant. After recrystallization in ethanol, ethyl 2-(3-methoxyphenyl)-4-quinazolinepropionate (1.5 g), m.p. 70° C., is obtained.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04788204 |
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| 出典データセット | uspto-grants-1988_11 |
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| ORD ID | ord-718be82b29314e4eb59ec196f96c8a45 |
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| 出典メモ | uspto-grants-1988_11 |
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