Dimethylamine, hydrochloride → HCID 68415183, compound
Reaction equation
Cl.[CH2:2]([N:9]1[CH2:14][CH2:13][CH:12]([N:15]([CH3:27])[C:16](=[O:26])[CH2:17][O:18][C:19]2[CH:24]=[N:23][CH:22]=[C:21]([Cl:25])[N:20]=2)[CH2:11][CH2:10]1)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.Cl.[CH3:29][NH:30][CH3:31]>>[ClH:25].[CH2:2]([N:9]1[CH2:14][CH2:13][CH:12]([N:15]([CH3:27])[C:16](=[O:26])[CH2:17][O:18][C:19]2[CH:24]=[N:23][CH:22]=[C:21]([N:30]([CH3:31])[CH3:29])[N:20]=2)[CH2:11][CH2:10]1)[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1Participants
3
Procedure
The title compound was synthesized from Compound 129 and dimethylamine hydrochloride in the same manner as in Example 130.
Sources & evidence
- ORD record
- ord-bb25e4adc7af44cbb12548238821a062
- Source dataset
- uspto-grants-2014_04
- Patent number
- US08685989B2
Reaction notes
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