4-(4-Ethyl-4H-[1,2,4]triazol-3-yl)-pyridine → 5-(3,5-Difluoro-phenyl)-4-methyl-4H-[1,2,4]triazole-3-carbaldehyde
반응식
C(N1C=NN=C1C1C=CN=CC=1)C.C(N1C(C2C=CN=CC=2)=NN=C1[CH2:27][OH:28])C.C(N1C(C2C=CN=CC=2)=NN=C1C=O)C.[F:44][C:45]1[CH:46]=[C:47]([C:52]2[N:53]([CH3:58])[C:54](=S)[NH:55][N:56]=2)[CH:48]=[C:49]([F:51])[CH:50]=1>>[F:44][C:45]1[CH:46]=[C:47]([C:52]2[N:53]([CH3:58])[C:54]([CH:27]=[O:28])=[N:55][N:56]=2)[CH:48]=[C:49]([F:51])[CH:50]=1참가 물질
5
반응물 4
생성물 1
실험 절차
The title compound is prepared analogously to the sequence described for 4-(4-ethyl-4H-[1,2,4]triazol-3-yl)-pyridine (example 21), (4-ethyl-5-pyridin-4-yl-4H-[1,2,4]triazol-3-yl)-methanol (example 22), and 4-ethyl-5-pyridin-4-yl-4H-[1,2,4]triazole-3-carbaldehyde (example 23a) by using 5-(3,5-Difluoro-phenyl)-4-methyl-2,4-dihydro-[1,2,4]triazole-3-thione as starting material.
출처 및 근거
- ORD 기록
- ord-147efc5ca17a4fd48e573dca337ea308
- 출처 데이터셋
- uspto-grants-2010_04
- 특허 번호
- US07691892B2
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