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(S)-2-tert-butoxycarbonylamino-3-difluoromethoxy-propionic acid benzyl ester → (S)-2-tert-Butoxycarbonylamino-3-difluoromethoxy-propionic acid
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | (S)-2-tert-butoxycarbonylamino-3-difluoromethoxy-propionic acid benzyl ester | HCID 90041473 | — |
| 触媒 | Palladium | HCID 23938 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | (S)-2-tert-Butoxycarbonylamino-3-difluoromethoxy-propionic acid | HCID 86709693 | 100.1% |
反応手順
A solution of the compound of Formula XIII(a), (S)-2-tert-butoxycarbonylamino-3-difluoromethoxy-propionic acid benzyl ester (1.76 g, 5.09 mmol) in THF was stirred with 10% Pd/C (360 mg) under a hydrogen atmosphere for 2 hours. The reaction mixture was filtered and concentrated to give the compound of Formula IV(a), (S)-2-tert-butoxycarbonylamino-3-difluoromethoxy-propionic acid (1.3 g, 100%) as a sticky, colorless oil. 1H NMR (300 MHz, CDCl3): δ (ppm) 6.21 (wt, 1H), 5.35 (d, 1H), 4.59 (m, 1H), 4.35 (m, 1H), 4.21 (m, 1H) and 1.42 (s, 9H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09441012B2 |
| 出典データセット | uspto-grants-2016_09 |
| ORD ID | ord-7594e7f9c27343a4a2c736838633cf8d |
| 出典メモ | uspto-grants-2016_09 |