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Ethyl Acetate → 3-(1-Aminoethyl)-3-hydroxypyrrolidine-1-carboxylic acid benzyl ester
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | Ammonium Hydroxide | HCID 14923 | — |
| 反応物 | Benzyl 2-methyl-1-oxa-5-azaspiro[2.4]heptane-5-carboxylate | HCID 21041146 | — |
| 溶媒 | Methanol | HCID 887 | — |
| 生成物 | 3-(1-Aminoethyl)-3-hydroxypyrrolidine-1-carboxylic acid benzyl ester | HCID 69068640 | — |
反応手順
A solution of 2-methyl-1-oxa-5-azaspiro[2,4]heptane-5-carboxylic acid benzyl ester (Example A9, 0.31 g, 1.25 mmol) in methanol (10 mL) and ammonium hydroxide (7 mL) is heated in a sealed tube at 100° C. for 16 hours. After cooling, the reaction mixture is dissolved ethyl acetate, washed with water, dried over Na2SO4 and evaporated to afford the title compound (0.340 g). 1H NMR (200 MHz, CDCl3): δ 7.33–7.26 (m, 5H), 5.28 (bs, 2H), 5.07 (s, 2H), 3.56–3.16 (m, 5H), 2.03–1.76 (m, 2H), 1.15 (d, 3H).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US07094780B1 |
| 出典データセット | uspto-grants-2006_08 |
| ORD ID | ord-25d841ff62cf41b6862babb19ab9536f |
| 出典メモ | uspto-grants-2006_08 |