2-Chloro-5-(chloromethyl)pyridine → {5-Methoxy-2-methyl-4-[6-(4-trifluoromethyl-phenyl)-pyridin-3-ylmethylsulfanyl]-phenoxy}-acetic acid
Reaction equation
ClC1C=CC(CCl)=CN=1.COC(=O)COC1C=C(OC)C(S)=CC=1C.C[O:27][C:28](=[O:58])[CH2:29][O:30][C:31]1[CH:36]=[C:35]([O:37][CH3:38])[C:34]([S:39][CH2:40][C:41]2[CH:42]=[N:43][C:44]([C:47]3[CH:52]=[CH:51][C:50]([C:53]([F:56])([F:55])[F:54])=[CH:49][CH:48]=3)=[CH:45][CH:46]=2)=[CH:33][C:32]=1[CH3:57]>>[CH3:38][O:37][C:35]1[C:34]([S:39][CH2:40][C:41]2[CH:42]=[N:43][C:44]([C:47]3[CH:48]=[CH:49][C:50]([C:53]([F:56])([F:55])[F:54])=[CH:51][CH:52]=3)=[CH:45][CH:46]=2)=[CH:33][C:32]([CH3:57])=[C:31]([CH:36]=1)[O:30][CH2:29][C:28]([OH:58])=[O:27]Participants
4
Reactant 3
Product 1
Procedure
The title compound was prepared from 2-Chloro-5-chloromethyl-pyridine and 1D in a manner analogous to Example 1F. MS m/z 370 (M+2). Step 2. Preparation of {5-Methoxy-2-methyl-4-[6-(4-trifluoromethyl-phenyl)-pyridin-3-ylmethylsulfanyl]-phenoxy}-acetic acid methyl ester (Compound 19B)
Sources & evidence
- ORD record
- ord-eafb46104020444ea3e18ae55255d0ec
- Source dataset
- uspto-grants-2005_11
- Patent number
- US06964983B2
Reaction notes
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