Isobutyryl chloride → HCID 11411101、化合物
反応式
[CH3:1][CH:2]1[CH:27]2[O:28][C:26]2([CH3:29])[CH:25]([OH:30])[CH2:24][C:22](=[O:23])[N:21]([CH3:31])[C:14]2=[C:15]([Cl:20])[C:16]([O:18][CH3:19])=[CH:17][C:12](=[CH:13]2)[CH2:11][C:10]([CH3:32])=[CH:9][CH:8]=[CH:7][CH:6]([O:33][CH3:34])[C:5]2([OH:39])[NH:35][C:36]([O:38][CH:3]1[CH2:4]2)=[O:37].[C:40](Cl)(=[O:44])[CH:41]([CH3:43])[CH3:42]>C(N(CC)CC)C.CN(C)C=O>[CH3:1][C@H:2]1[C@H:27]2[O:28][C@@:26]2([CH3:29])[C@@H:25]([O:30][C:40]([CH:41]([CH3:43])[CH3:42])=[O:44])[CH2:24][C:22](=[O:23])[N:21]([CH3:31])[C:14]2=[C:15]([Cl:20])[C:16]([O:18][CH3:19])=[CH:17][C:12](=[CH:13]2)[CH2:11][C:10]([CH3:32])=[CH:9][CH:8]=[CH:7][C@@H:6]([O:33][CH3:34])[C@:5]2([OH:39])[NH:35][C:36]([O:38][C@H:3]1[CH2:4]2)=[O:37]参加物
5
実験手順
In a mixture of 1 ml triethylamine and 50 ml of dimethylformamide was dissolved 100 mg of maytansinol and, while the solution was stirred under ice-cooling, 50 μl of isobutyryl chloride was added dropwise. The mixture was stirred under ice-cooling for 30 minutes and then, at room temperature for 2.5 hours, after which it was distilled under reduced pressure. The residue was dissolved in 10 ml of dichloromethane, washed with water and dried (Na2SO4). The solvent was distilled off under reduced pressure and the residue was chromatographed and recrystallized as in Reference Example 1. By the above procedure there was obtained 19.4 mg of Ansamitocin P-3.
後処理
- temperaturecooling
- stirringThe mixture was stirred under ice-
- temperaturecooling for 30 minutes
- distillationafter which it was distilled under reduced pressure
- dissolutionThe residue was dissolved in 10 ml of dichloromethane
- washwashed with water
- dry with materialdried (Na2SO4)
- distillationThe solvent was distilled off under reduced pressure
- customthe residue was chromatographed
- customrecrystallized as in Reference Example 1
出典と根拠
- ORDレコード
- ord-08fec8384f1b44fa9ceab019bf2f0714
- 出典データセット
- uspto-grants-1981_05
- 特許番号
- US04265814
反応ノート
読み込み中…