(4-Fluoro-2-methylphenyl)boronic acid → HCID 59518060, compound
Reaction equation
C[O:2][C:3](=[O:32])[CH2:4][CH2:5][NH:6][C:7](=[O:31])[C:8]1[CH:13]=[CH:12][C:11]([CH:14]([O:21][C:22]2[CH:27]=[C:26]([CH3:28])[C:25](Br)=[C:24]([CH3:30])[CH:23]=2)[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20])=[CH:10][CH:9]=1.[F:33][C:34]1[CH:39]=[CH:38][C:37](B(O)O)=[C:36]([CH3:43])[CH:35]=1>>[F:33][C:34]1[CH:39]=[CH:38][C:37]([C:25]2[C:26]([CH3:28])=[CH:27][C:22]([O:21][CH:14]([C:11]3[CH:10]=[CH:9][C:8]([C:7]([NH:6][CH2:5][CH2:4][C:3]([OH:2])=[O:32])=[O:31])=[CH:13][CH:12]=3)[CH2:15][CH2:16][CH2:17][CH2:18][CH2:19][CH3:20])=[CH:23][C:24]=2[CH3:30])=[C:36]([CH3:43])[CH:35]=1Participants
3
Procedure
This compound is made in a manner substantially similar to Example 117 using isomer 1 of 3-{4-[1-(4-bromo-3,5-dimethyl-phenoxy)-heptyl]-benzoylamino}-propionic acid methyl ester and 4-fluoro-2-methyl-phenylboronic acid as starting materials in step D. MS (ES): 520.2 [M+H]+.
Sources & evidence
- ORD record
- ord-23de5085b6b2467d9b0a263ca0a029c1
- Source dataset
- uspto-grants-2010_10
- Patent number
- US07816557B2
Reaction notes
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