Benzylamine → HCID 25235490, compound
Reaction equation
Cl[C:2]1[CH:11]=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7](Cl)[CH:8]=2)[N:3]=1.[CH3:13][O:14][C:15]1[CH:22]=[CH:21][CH:20]=[CH:19][C:16]=1[CH2:17][NH2:18].[CH2:23]([NH2:30])[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1>>[CH2:23]([NH:30][C:7]1[CH:8]=[C:9]2[C:4](=[CH:5][CH:6]=1)[N:3]=[C:2]([NH:18][CH2:17][C:16]1[CH:19]=[CH:20][CH:21]=[CH:22][C:15]=1[O:14][CH3:13])[CH:11]=[CH:10]2)[C:24]1[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=1Participants
4
Procedure
The title compound, MS: m/e=369.9 (M+H+), was prepared in accordance with the general method of example 1 from 2,6-dichloroquinoline, 2-methoxybenzylamine and benzylamine.
Sources & evidence
- ORD record
- ord-5a53ac6be5674716b70a07d2b14b6a45
- Source dataset
- uspto-grants-2013_03
- Patent number
- US08399674B2
Reaction notes
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