関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Piperidine | HCID 8082 | — |
| 反応物 | 6-Amino-5-fluoroindolin-2-one | HCID 10103504 | — |
| 反応物 | (1S)-2-Chloro-1-methyl-2-oxoethyl acetate | HCID 11094804 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | acetic acid 1-(5-fluoro-2-oxo-2,3-dihydro-1H-indol-6-ylcarbamoyl)-ethyl ester | HCID 59250052 | 99% |
反応手順
The stirred solution of 5-fluoro-6-amino-1,3-dihydro-indol-2-one (450 mg, 2.71 mmol) in 10 ml of tetrahydrofuran was added with piperidine (0.4 ml). The mixture was cooled to −40° C. in an acetone-dry ice bath and added with (S)-acetic acid 1-chlorocarbonyl-ethyl ester (423 mg, 2.71 mmol) in 10 ml of tetrahydrofuran dropwise. Upon the completion of the addition, the resulting mixture was stirred at the room temperature overnight until the precipitate was formed. The solid was filtered, washed with water and recrystallized from methanol to give acetic acid 1-(5-fluoro-2-oxo-2,3-dihydro-1H-indol-6-ylcarbamoyl)-ethyl ester (750 mg, 99%) as a white solid.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08362251B2 |
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| 出典データセット | uspto-grants-2013_01 |
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| ORD ID | ord-99891e0c6d4f4e6999c9704203a79592 |
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| 出典メモ | uspto-grants-2013_01 |
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