Cyclopropanemethanol → 5-(4-Fluorophenyl)-6-cyclopropylmethoxy-nicotinic acid
Reaction equation
Cl[C:2]1[C:10]([C:11]2[CH:16]=[CH:15][C:14]([F:17])=[CH:13][CH:12]=2)=[CH:9][C:5]([C:6]([OH:8])=[O:7])=[CH:4][N:3]=1.[OH:18][CH2:19][CH:20]1[CH2:22][CH2:21]1>>[F:17][C:14]1[CH:15]=[CH:16][C:11]([C:10]2[C:2]([O:18][CH2:19][CH:20]3[CH2:22][CH2:21]3)=[N:3][CH:4]=[C:5]([CH:9]=2)[C:6]([OH:8])=[O:7])=[CH:12][CH:13]=1Participants
3
Procedure
The title compound was synthesized in analogy to Example 5c, using 6-chloro-5-(4-fluoro-phenyl)-nicotinic acid and (hydroxymethyl)cyclopropane as starting materials, MS (ISP) 286.0 (M−H).
Sources & evidence
- ORD record
- ord-a3c40af9bddf4f60ad24f5b8970d837f
- Source dataset
- uspto-grants-2010_10
- Patent number
- US07812028B2
Reaction notes
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