참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Methanol | HCID 887 | — |
| 반응물 | 4-[(3-Fluorophenyl)methoxy]benzaldehyde | HCID 880119 | — |
| 반응물 | (2R)-2-Aminopropanamide hydrochloride | HCID 2775814 | — |
| 용매 | Triethylamine | HCID 8471 | — |
| 생성물 | (R)-2-[4-(3-Fluorobenzyloxy)benzylideneamino]propanamide | HCID 42636153 | 49.1% |
반응 단계
In a 250 mL, 4 necked round bottom flask, equipped with mechanical stirrer, thermometer, reflux condenser and under a flow of nitrogen, D-alaninamide hydrochloride (6.1 g) and methanol (80 mL) are charged and stirred for 15 min at 20° C. Triethylamine (5 g) is added at such a rate that the temperature remains below 30° C. The mixture is stirred for 10 min, whereupon solid 4-(3-fluorobenzyloxy)benzaldehyde (10 g, Example 10b) is added portion wise in about 30 min. After stirring for 3 hours at 20° C., the mixture is cooled to 5° C. After stirring for 3 hours at this temperature, the solid is filtered and washed with small amount of pre-cooled methanol. The wet solid is dried under vacuum for 12 hours a 25° C., yielding 6.4 g of title compound as white solid, with 46.4% yield; m.p 111.9.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08846763B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-5820c3f822c94d19be155428f632981c |
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| 출처 메모 | uspto-grants-2014_09 |
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