関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | Formic Acid | HCID 284 | — |
| 反応物 | Isopropanol | HCID 3776 | — |
| 反応物 | 3-Pyridinepropanoic acid, beta-oxo-, methyl ester | HCID 108645 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | Methyl 3-amino-3-(pyridin-3-YL)prop-2-enoate | HCID 69944552 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06515130B1 |
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| 出典データセット | uspto-grants-2003_02 |
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| ORD ID | ord-3fa5e721e718439b9d7e1fad80c683ca |
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| 出典メモ | uspto-grants-2003_02 |
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