Benzylamine → HCID 25235661, compound
Reaction equation
C([NH:4][C:5]1[C:14]2[C:9](=[CH:10][CH:11]=[C:12](Cl)[CH:13]=2)[N:8]=[C:7]([NH:16][CH2:17][C:18]2[O:19][C:20]([CH3:23])=[CH:21][CH:22]=2)[CH:6]=1)C=C.[CH2:24]([NH2:31])[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1>>[CH2:24]([NH:31][C:12]1[CH:13]=[C:14]2[C:9](=[CH:10][CH:11]=1)[N:8]=[C:7]([NH:16][CH2:17][C:18]1[O:19][C:20]([CH3:23])=[CH:21][CH:22]=1)[CH:6]=[C:5]2[NH2:4])[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1Participants
3
Procedure
The title compound, MS: m/e=359.2 (M+H+), was prepared in accordance with the general method of example 44 from N4-allyl-6-chloro-N2-(5-methyl-furan-2-ylmethyl)-quinoline-2,4-diamine and benzylamine.
Sources & evidence
- ORD record
- ord-a55aef0cdf814af0a7f871cab7744747
- Source dataset
- uspto-grants-2013_03
- Patent number
- US08399674B2
Reaction notes
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