関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Hydrazine hydrate (1:1) | HCID 24654 | — |
| 反応物 | 2-(2-Chloro-4-methoxyphenyl)-3-oxobutanenitrile | HCID 22178154 | — |
| 溶媒 | Acetic Acid | HCID 176 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | HCID 178488693 | HCID 178488693 | — |
反応手順
Under argon gas atmosphere, to a solution of the compound prepared in Example 1 (38.7 g) in toluene, acetic acid (14.5 mL) and 60% aqueous solution of hydrazine hydrate (17.7 mL) were sequentially added at 10 to 30° C. of internal temperature. The mixture was stirred for 7 hours at 45 to 55° C. of internal temperature. To the reaction solution cooled to 10 to 30° C. of internal temperature, 2 mol/L hydrochloric acid was added and then the mixture was separated. The aqueous layer was adjusted to pH 6.5 to 7.5 by adding 25 wt % sodium hydroxide. Isopropyl acetate (216 mL) was added to the adjusted aqueous layer. The separated organic layer was concentrated under reduced pressure. The residue was heated, and n-heptane was added. The solution was cooled to 10 to 30° C. of internal temperature. After the crystal was precipitated, the solution was stirred for 30 minutes. Furthermore, n-heptane was added to the solution, and the mixture was stirred for 1 hour. The precipitated crystal was collected by filtration, dried under reduced pressure for 14 hours or more at about 50° C. to give the title compound having the following physical data (35.5 g (94.8 area %); quantitative value: 61% (2 processes)).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07947697B1 |
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| 出典データセット | uspto-grants-2011_05 |
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| ORD ID | ord-23cbb45c906a43a8bfaa30078cb036cc |
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| 出典メモ | uspto-grants-2011_05 |
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