Isobutyl chloroformate → (Z)-isobutyl (2-(5-(4-ethoxybenzylidene)-2,4-dioxothiazolidin-3-yl)ethyl)carbamate
反応式
[NH2:1][CH2:2][CH2:3][N:4]1[C:8](=[O:9])/[C:7](=[CH:10]/[C:11]2[CH:16]=[CH:15][C:14]([O:17][CH2:18][CH3:19])=[CH:13][CH:12]=2)/[S:6][C:5]1=[O:20].Cl[C:22]([O:24][CH2:25][CH:26]([CH3:28])[CH3:27])=[O:23].CCN(C(C)C)C(C)C.C(OC1C=CC(/C=C2/C(=O)N(CCNC(=O)C)C(=O)S/2)=CC=1)C>>[CH2:18]([O:17][C:14]1[CH:15]=[CH:16][C:11](/[CH:10]=[C:7]2/[C:8](=[O:9])[N:4]([CH2:3][CH2:2][NH:1][C:22](=[O:23])[O:24][CH2:25][CH:26]([CH3:28])[CH3:27])[C:5](=[O:20])[S:6]/2)=[CH:12][CH:13]=1)[CH3:19]参加物
5
反応物 4
生成物 1
実験手順
The title compound 26c was prepared from compound 76 (70 mg, 0.17 mmol), isobutyl chloroformate (25 μL, 0.19 mmol) and DIPEA (75 μL, 0.43 mmol) in a manner similar to that described for 25a in 96.4% (65 mg) yield as a light-yellow solid.
後処理
- customyield as a light-yellow solid
出典と根拠
- ORDレコード
- ord-9730467e9dde4962b6d4a1e1fc08e78e
- 出典データセット
- uspto-grants-2015_08
- 特許番号
- US09115122B2
反応ノート
読み込み中…