Neopentylamine → HCID 54401596, compound
Reaction equation
[C:1]([O:5][C:6]([N:8]([C:31]1[CH:36]=[CH:35][N:34]=[CH:33][CH:32]=1)[CH2:9][CH2:10][O:11][C:12]1[CH:13]=[C:14]([CH:27]=[C:28]([Cl:30])[CH:29]=1)[C:15]([N:17]([CH:22]([CH3:26])C(O)=O)[CH:18]1[CH2:21][CH2:20][CH2:19]1)=[O:16])=[O:7])([CH3:4])([CH3:3])[CH3:2].CN([C:40]([O:44]N1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CCN(C(C)C)C(C)C.[CH2:70]([NH2:75])[C:71]([CH3:74])([CH3:73])[CH3:72]>CN(C=O)C>[C:1]([O:5][C:6](=[O:7])[N:8]([CH2:9][CH2:10][O:11][C:12]1[CH:13]=[C:14]([C:15](=[O:16])[N:17]([CH:18]2[CH2:21][CH2:20][CH2:19]2)[CH2:22][CH2:26][C:40](=[O:44])[NH:75][CH2:70][C:71]([CH3:74])([CH3:73])[CH3:72])[CH:27]=[C:28]([Cl:30])[CH:29]=1)[C:31]1[CH:32]=[CH:33][N:34]=[CH:35][CH:36]=1)([CH3:4])([CH3:3])[CH3:2]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To a stirred solution of ({3-[2-(tert-butoxycarbonyl-pyridin-4-yl-amino)-ethoxy]-5-chloro-benzoyl}-cyclobutyl-amino)-propionic acid (0.025 g) and HATU® (0.038 g) in DMF (1 ml) was added DIPEA (0.017 ml) followed by neopentylamine (0.053 ml) after 10 min. The reaction mixture was stirred at room temperature for 18 h and then concentrated under reduced pressure. The residue was subjected to preparative hplc and the title compound (0.016 g) was obtained as a colourless gum by concentration of the required fraction under reduced pressure and drying by repetitive addition of acetonitrile and concentration under reduced pressure.
Workup
- concentrationconcentrated under reduced pressure
Sources & evidence
- ORD record
- ord-fa274a6cfb7343c3a104ba8d43b6ea39
- Source dataset
- uspto-grants-2001_12
- Patent number
- US06326386B1
Reaction notes
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