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Morpholine, 4-(chloroacetyl)- → Methyl 2-morpholin-4-yl-2-oxoethyl(2E)but-2-ene-1,4-dioate
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Morpholine, 4-(chloroacetyl)- | HCID 74040 | — |
| 反応物 | Cesium bicarbonate | HCID 2734983 | — |
| 反応物 | Monomethyl Fumarate | HCID 5369209 | — |
| 溶媒 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 生成物 | Methyl 2-morpholin-4-yl-2-oxoethyl(2E)but-2-ene-1,4-dioate | HCID 46179072 | 35% |
反応手順
Following general procedure A, methyl hydrogen fumarate (MHF) (0.50 g, 3.84 mmol) dissolved in NMP was reacted at ca. 55° C. with 4-(chloroacetyl) morpholine (0.75 g, 4.61 mmol) in the presence of CsHCO3 (0.89 g, 4.61 mmol) to afford 0.34 g (35% yield) of the title compound (3) as a white solid after purification by mass-guided preparative HPLC and lyophilization. M.p.: 124 to 126° C.; 1H NMR (CDCl3, 400 MHz): δ 6.97-6.91 (m, 2H), 4.84 (s, 2H), 3.82 (s, 3H), 3.72-3.70 (m, 4H), 3.64-3.62 (m, 2H), 3.46-3.41 (m, 2H). MS (ESI): m/z 258.04 (M+H)+.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US08785443B2 |
| 出典データセット | uspto-grants-2014_07 |
| ORD ID | ord-dcb5af68c8de4b4ca00ce33293101783 |
| 出典メモ | uspto-grants-2014_07 |