Dimethylamine → HCID 25106689, compound
Reaction equation
[NH2:1][C:2]1[C:11]2[N:12]=[C:13]([CH2:35][O:36][CH2:37][CH3:38])[N:14]([CH2:15][CH2:16][CH2:17][N:18]([CH2:23][C:24]3[CH:25]=[C:26]([CH2:30][C:31]([O:33][CH3:34])=[O:32])[CH:27]=[CH:28][CH:29]=3)[C:19](=[O:22])[CH2:20]Cl)[C:10]=2[C:9]2[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=2[N:3]=1.[CH3:39][NH:40][CH3:41]>CN(C=O)C>[CH3:34][O:33][C:31](=[O:32])[CH2:30][C:26]1[CH:27]=[CH:28][CH:29]=[C:24]([CH2:23][N:18]([CH2:17][CH2:16][CH2:15][N:14]2[C:10]3[C:9]4[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=4[N:3]=[C:2]([NH2:1])[C:11]=3[N:12]=[C:13]2[CH2:35][O:36][CH2:37][CH3:38])[C:19](=[O:22])[CH2:20][N:40]([CH3:41])[CH3:39])[CH:25]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The product from step (vi) (30 mg) was dissolved in DMF (2 mL) then a solution of dimethylamine (2M in THF, 0.279 mL) was added at rt under nitrogen. The resulting solution was stirred at rt for 16 h. The mixture was purified by RPHPLC to give the title compound, yield 4.5 mg.
Workup
- customThe mixture was purified by RPHPLC
Sources & evidence
- ORD record
- ord-fce58ec914cd4d119d2ac232c5bdee8a
- Source dataset
- uspto-grants-2013_05
- Patent number
- US08436178B2
Reaction notes
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