[6-(Trifluoromethyl)pyridin-2-yl]methanol → 3-[5-Chloro-2-(6-trifluoromethyl-pyridin-2-ylmethoxy)-phenoxy]-azetidine-1-carboxylic acid tert-butyl ester
Reaction equation
[F:1][C:2]([F:12])([F:11])[C:3]1[N:8]=[C:7]([CH2:9][OH:10])[CH:6]=[CH:5][CH:4]=1.[C:13]([O:17][C:18]([N:20]1[CH2:23][CH:22]([O:24][C:25]2[CH:30]=[C:29]([Cl:31])[CH:28]=[CH:27][C:26]=2O)[CH2:21]1)=[O:19])([CH3:16])([CH3:15])[CH3:14]>>[C:13]([O:17][C:18]([N:20]1[CH2:23][CH:22]([O:24][C:25]2[CH:30]=[C:29]([Cl:31])[CH:28]=[CH:27][C:26]=2[O:10][CH2:9][C:7]2[CH:6]=[CH:5][CH:4]=[C:3]([C:2]([F:11])([F:1])[F:12])[N:8]=2)[CH2:21]1)=[O:19])([CH3:16])([CH3:14])[CH3:15]Participants
3
Procedure
Prepared from the title compound of Step A and 3-(5-Chloro-2-hydroxy-phenoxy)-azetidine-1-carboxylic acid tert-butyl ester using general procedure 7.
Sources & evidence
- ORD record
- ord-ea259660f80349a780f6e0ca244905f9
- Source dataset
- uspto-grants-2014_02
- Patent number
- US08642583B2
Reaction notes
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