関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Triethylamine | HCID 8471 | — |
| 反応物 | Bromoacetyl chloride | HCID 89602 | — |
| 反応物 | N-cycloheptyl-N-methylamine | HCID 276275 | — |
| 反応物 | 8-[3-(N-glycyl-N-methylamino)2,6-dichlorobenzyloxy]-2-methylquinoline | HCID 11795484 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | HCID 22112924 | HCID 22112924 | — |
反応手順
To a mixture of 8-[3-(N-glycyl-N-methylamino)-2,6-dichlorobenzyloxy]-2-methylquinoline (150 ml), triethylamine (0.077 ml) and dichloromethane (1.5 ml) was added bromoacetyl chloride (0.034 ml) in a dry ice-acetone bath. After 30 minutes, to the mixture was added N-methyl-N-cycloheptylamine (236 mg). The mixture was stirred for 3 hours at ambient temperature. The reaction mixture was washed with aqueous sodium bicarbonate solution, water and brine. The organic layer was dried over magnesium sulfate and evaporated in vacuo. The residue was purified .by a silica gel column chromatography (dichloromethane--methanol) to yield 8-[3-[N-[(N-cycloheptyl-N-methylglycyl)glycyl]-N-methylamino]-2,6-dichlorobenzyloxy]-2-methylquinoline (151 mg) as amorphous.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 特許番号 | US05922711 |
|---|
| 出典データセット | uspto-grants-1999_07 |
|---|
| ORD ID | ord-85b66600864046699ef0d471c959932f |
|---|
| 出典メモ | uspto-grants-1999_07 |
|---|