반응식
[NH2:1][C:2]1[N:7]=[C:6]([C:8]2[O:9][CH:10]=[CH:11][CH:12]=2)[C:5]([C:13]#[N:14])=[C:4](OS(C(F)(F)F)(=O)=O)[CH:3]=1.Cl.[NH2:24][CH2:25][C:26]1[C:31]([Cl:32])=[CH:30][C:29]([C:33]([F:36])([F:35])[F:34])=[CH:28][N:27]=1.C1CCN2C(=NCCC2)CC1>COCCOC>[NH2:1][C:2]1[CH:3]=[C:4]([NH:24][CH2:25][C:26]2[C:31]([Cl:32])=[CH:30][C:29]([C:33]([F:36])([F:35])[F:34])=[CH:28][N:27]=2)[C:5]([C:13]#[N:14])=[C:6]([C:8]2[O:9][CH:10]=[CH:11][CH:12]=2)[N:7]=1참가 물질
5
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
From trifluoromethanesulfonic acid 6-amino-3-cyano-2-furan-2-yl-pyridin-4-yl ester, 2-aminomethyl-3-chloro-5-(trifluoromethyl)pyridine hydrochloride and DBU in DME. ES-MS m/e (%): 396 (M{37Cl}+H+, 40), 394 (M{35C}+H+, 100).
출처 및 근거
- ORD 기록
- ord-ea62995acad04f12a478a3b07e7dd2d3
- 출처 데이터셋
- uspto-grants-2003_07
- 특허 번호
- US06586441B2
연결된 노트
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