반응식
[NH2:1][C:2]1[N:7]=[C:6]([CH3:8])[CH:5]=[CH:4][N:3]=1.[CH:9]1([N+:15]#[C-:16])[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]1.[CH3:17][N:18]1[CH:22]=[CH:21][CH:20]=[C:19]1[CH:23]=O>Cl(O)(=O)(=O)=O>[CH:9]1([NH:15][C:16]2[N:3]3[CH:4]=[CH:5][C:6]([CH3:8])=[N:7][C:2]3=[N:1][C:23]=2[C:19]2[N:18]([CH3:17])[CH:22]=[CH:21][CH:20]=2)[CH2:14][CH2:13][CH2:12][CH2:11][CH2:10]1참가 물질
5
실험 절차
Compound (38) was prepared according to the general synthesis instructions from 1.0 ml of 2-amino-4-methylpyrimidine solution (0.1 M, DCM), 0.575 ml of cyclohexyl isocyanide solution (0.2 M, DCM), 0.500 ml of N-methylpyrrole-2-carbaldehyde solution (0.3 M, DCM), and 10 μl of perchloric acid (w=20%).
출처 및 근거
- ORD 기록
- ord-9a13c14e378f4b7cabd9e4ac51904452
- 출처 데이터셋
- uspto-grants-2005_02
- 특허 번호
- US06849642B2
연결된 노트
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