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2,5-dioxopyrrolidin-1-yl 3-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)propanoate → 3-(2,5-dioxo-2H-pyrrol-1(5H)-yl)-N-(3-(1,1,1,3,3,3-hexafluoro-2-(methoxy-methoxy)propan-2-yl)-4-(tributylstannyl)benzyl)-N-methylpropanamide
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2,5-dioxopyrrolidin-1-yl 3-(2,5-dioxo-2,5-dihydro-1H-pyrrol-1-yl)propanoate | HCID 4620597 | — |
| 反応物 | HCID 87358059 | HCID 87358059 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 3-(2,5-dioxo-2H-pyrrol-1(5H)-yl)-N-(3-(1,1,1,3,3,3-hexafluoro-2-(methoxy-methoxy)propan-2-yl)-4-(tributylstannyl)benzyl)-N-methylpropanamide | HCID 87359001 | 81% |
反応手順
Compound 14 (86 mg, 138 μmol) was dissolved in anhydrous acetonitrile (2 mL) and 3-(Maleimido)propionic acid N-hydroxysuccinimide ester (44 mg, 166 mmol) was added. The mixture was stirred overnight at room temperature, the solvent removed under reduced pressure and the residue purified over silica gel using chloroform/methanol (98/2) as eluant to give 86 mg (111 μmol, 81% yield) of a colorless oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US09290421B2 |
| 出典データセット | uspto-grants-2016_03 |
| ORD ID | ord-43ab1602f6f2477299f955d41861f645 |
| 出典メモ | uspto-grants-2016_03 |