참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ammonia | HCID 222 | — |
| 반응물 | Formic Acid | HCID 284 | — |
| 반응물 | Isopropanol | HCID 3776 | — |
| 반응물 | 3-Pyridinepropanoic acid, beta-oxo-, methyl ester | HCID 108645 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | Methyl 3-amino-3-(pyridin-3-YL)prop-2-enoate | HCID 69944552 | — |
반응 단계
Methyl nicotinoylacetate (88 g, 0.5 mol) was dissolved in toluene (200 g), isopropyl alcohol (200 g), and formic acid (98-100%, 1.22 g, 0.03 mol) and heated to 60-65° C. Gaseous ammonia (23 g, 1.35 mol) was bubbled through the solution for 15 minutes. The white suspension was stirred at 65° C. until a homogeneous solution formed. The solution was stirred for two hours at 65° C. and then concentrated (ca. 200 g) at 65° C. The residue was cooled to −5° C. with stirring and methyl 3-amino-3-(3-pyridyl)-2-propenoate crystallized as colorless needles. The process of reducing the volume to 50% followed by cooling was repeated three times with the mother liquors. Filtration, washing with toluene, and drying at 30° C. resulted in 77.74 g (88.8%) of methyl 3-amino-3-(3-pyridyl)-2-propenoate as colorless crystals.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06515130B1 |
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| 출처 데이터셋 | uspto-grants-2003_02 |
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| ORD ID | ord-3fa5e721e718439b9d7e1fad80c683ca |
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| 출처 메모 | uspto-grants-2003_02 |
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