化工社化工社 化学情報印刷レポート · 研究参考用
HRID 17314作成日:2026年10月26日
(3S)-(-)-3-(Dimethylamino)pyrrolidine → 7-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-2-(methoxymethyl)-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrile
https://huagongshe.com/reaction/17314
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | (3S)-(-)-3-(Dimethylamino)pyrrolidine | HCID 7019156 | — |
| 反応物 | 7-Fluoro-2-(methoxymethyl)-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrile | HCID 68585115 | — |
| 反応物 | Sodium bicarbonate water | HCID 86585896 | — |
| 溶媒 | Dimethyl Sulfoxide | HCID 679 | — |
| 生成物 | 7-[(3S)-3-(dimethylamino)pyrrolidin-1-yl]-2-(methoxymethyl)-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrile | HCID 68584472 | 17% |
反応手順
(3S)-3-(Dimethylamino)pyrrolidine (76 μl, 0.60 mmol) was added to a dimethyl sulfoxide (4 ml) solution of 7-fluoro-2-(methoxymethyl)-5-methyl-6-phenyl-1,3-benzoxazole-4-carbonitrile (I-59) (58 mg, 0.20 mmol), followed by stirring at 90° C. for 1 hour. After cooling to room temperature, the above brown oily substance and saturated sodium bicarbonate water were added, followed by extraction three times with ethyl acetate, the organic layer was washed with saturated brine, then dried over anhydrous magnesium sulfate. After filtration and concentration under reduced pressure, the resulting residue was subjected to column chromatography, and the eluate with chloroform:methanol (50:1) was concentrated under reduced pressure, the residue was dissolved in ethyl acetate, washed twice with saturated brine, then dried over anhydrous magnesium sulfate. After filtration and concentration tinder reduced pressure, the entitled compound (39 mg, 17%) was obtained as a brown oily substance.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US07737166B2 |
|---|
| 出典データセット | uspto-grants-2010_06 |
|---|
| ORD ID | ord-b341d755573047dcac0d67357cf083fb |
|---|
| 出典メモ | uspto-grants-2010_06 |
|---|