2-(Benzyloxy)pyridine-4-carboxylic acid → 2-(2-Benzyloxy-pyridin-4-yl)-3-(2,4-dichloro-phenyl)-1,1,1-trifluoro-butan-2-ol
반응식
COC(=O)CC1C=CC([C:11]([F:14])([F:13])[F:12])=CC=1Cl.C1(COC2C=C(C(O)=O)C=CN=2)C=CC=CC=1.[CH2:34]([O:41][C:42]1[CH:47]=[C:46]([C:48](=[O:59])[CH:49]([C:51]2[CH:56]=[CH:55][C:54]([Cl:57])=[CH:53][C:52]=2[Cl:58])[CH3:50])[CH:45]=[CH:44][N:43]=1)[C:35]1[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=1>N1C=CC=CC=1>[CH2:34]([O:41][C:42]1[CH:47]=[C:46]([C:48]([OH:59])([CH:49]([C:51]2[CH:56]=[CH:55][C:54]([Cl:57])=[CH:53][C:52]=2[Cl:58])[CH3:50])[C:11]([F:14])([F:13])[F:12])[CH:45]=[CH:44][N:43]=1)[C:35]1[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=1참가 물질
5
반응물 3
생성물 1
시약·촉매·용매 1
실험 절차
The title compound was prepared in analogy to the reaction sequence outlined in Example 1, steps 2 to 5, from 2-chloro-4-(trifluoromethyl)-benzeneacetic acid methyl ester and 2-(phenylmethoxy)-4-pyridinecarboxylic acid with the following modification: In the methylation step (Example 1, step 4), an inseparable mixture of the desired intermediate 1-(2-benzyloxy-pyridin-4-yl)-2-(2,4-dichloro-phenyl)-propan-1-one with the dimethylated compound 2-benzyloxy-4-[(E or Z)-2-(2,4-dichloro-phenyl)-1-methoxy-propenyl]-pyridine was obtained. This mixture was treated as follows:
후처리
- customwas obtained
- additionThis mixture was treated
출처 및 근거
- ORD 기록
- ord-6fe96ef319544dbe9d2a2c5d67605954
- 출처 데이터셋
- uspto-grants-2012_03
- 특허 번호
- US08143280B2
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