반응식
[CH3:1][C:2]1[C:12]2[CH:11]=[CH:10][C:9]3[CH:13]=[C:14]([CH3:17])[CH:15]=[CH:16][C:8]=3[CH:7]([C:18]3[C:19](=[O:25])[NH:20][C:21](=[O:24])[NH:22][CH:23]=3)[C:6]=2[CH:5]=[CH:4][C:3]=1[CH3:26].[CH2:27]([O:29][C:30]([C:32]1[O:33][C:34]([CH2:37]Br)=[CH:35][CH:36]=1)=[O:31])[CH3:28]>>[CH3:1][C:2]1[C:12]2[CH:11]=[CH:10][C:9]3[CH:13]=[C:14]([CH3:17])[CH:15]=[CH:16][C:8]=3[CH:7]([C:18]3[C:19](=[O:25])[NH:20][C:21](=[O:24])[N:22]([CH2:37][C:34]4[O:33][C:32]([C:30]([O:29][CH2:27][CH3:28])=[O:31])=[CH:36][CH:35]=4)[CH:23]=3)[C:6]=2[CH:5]=[CH:4][C:3]=1[CH3:26]참가 물질
3
반응물 2
생성물 1
실험 절차
The subtitle compound was prepared from the product of step (v) (0.95 g) and 5-bromomethyl-2-furancarboxylic acid ethyl ester (J. Chem. Soc. Perkin Trans. 1, 1981, 1125, Bull. Chem. Soc. Jpn. 1987, 60, 1807)(0.64 g) according to the method of example 1 step (iv). Purification was by chromatography eluting with 20% ethyl acetate in toluene. Yield 1.02 g.
후처리
- customPurification
- washeluting with 20% ethyl acetate in toluene
출처 및 근거
- ORD 기록
- ord-965eb5b2f5714489bb2ddb2ab8110335
- 출처 데이터셋
- uspto-grants-2000_12
- 특허 번호
- US06162808
연결된 노트
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