반응식
C[C:2]1([CH3:10])[CH2:7][CH2:6][CH2:5][C:4]([CH3:9])(C)N1.[CH3:11][C:12](=[O:17])[CH2:13][C:14](=[O:16])[CH3:15]>C(N(CC)CC)C>[C:4]1([CH:9]=[CH:11][C:12](=[O:17])[CH2:13][C:14](=[O:16])[CH3:15])[CH:5]=[CH:6][CH:7]=[CH:2][CH:10]=1참가 물질
4
실험 절차
The title compound was prepared by the method of Example 6 (that is, using 2,2,6,6-tetramethylpiperidine as base instead of triethylamine) using 2,4-pentanedione instead of ethyl acetoacetate. The material prepared by this procedure was identical to that prepared by the method of Example 30, as indicated by the reverse phase chromatographic method described in Example 2.
후처리
- customThe material prepared by this procedure
- customthat prepared by the method of Example 30
출처 및 근거
- ORD 기록
- ord-cd2210dc9bc94e0b894a0c50c8a286e9
- 출처 데이터셋
- uspto-grants-1987_03
- 특허 번호
- US04649157
연결된 노트
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