HCID 44482119, compound → HCID 44479292, compound
Reaction equation
C([O:8][C:9](=[O:36])[CH2:10][C@@H:11]([NH:16][C:17](=[O:35])[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][O:26][CH2:27][CH2:28][C:29]1[CH:34]=[CH:33][CH:32]=[CH:31][CH:30]=1)[CH2:12][N:13]([CH3:15])[CH3:14])C1C=CC=CC=1.CN(C)C[C@H](NC(=O)CCCCCCCCOC1C=CC=CC=1F)CC(O)=O>>[CH3:15][N:13]([CH3:14])[CH2:12][C@H:11]([NH:16][C:17](=[O:35])[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][O:26][CH2:27][CH2:28][C:29]1[CH:30]=[CH:31][CH:32]=[CH:33][CH:34]=1)[CH2:10][C:9]([OH:36])=[O:8]Participants
3
Procedure
Hydrogenation of (R)-4-dimethylamino-3-(9-phenethyloxy-nonanoylamino)-butyric acid benzyl ester in analogy with example 1, step 4 produced (R)-4-dimethylamino-3-[9-(2-fluoro-phenoxy)-nonanoylamino]-butyric acid. White solid, m/e=405.6 ([M−H]−).
Sources & evidence
- ORD record
- ord-503ac6e8eceb4934af986c93dc7c074d
- Source dataset
- uspto-grants-2013_01
- Patent number
- US08344027B2
Reaction notes
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