3-Pyridinemethanamine → HCID 25235660, 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.[N:24]1[CH:29]=[CH:28][CH:27]=[C:26]([CH2:30][NH2:31])[CH:25]=1>>[CH3:23][C:20]1[O:19][C:18]([CH2:17][NH:16][C:7]2[CH:6]=[C:5]([NH2:4])[C:14]3[C:9](=[CH:10][CH:11]=[C:12]([NH:31][CH2:30][C:26]4[CH:25]=[N:24][CH:29]=[CH:28][CH:27]=4)[CH:13]=3)[N:8]=2)=[CH:22][CH:21]=1Participants
3
Procedure
The title compound, MS: m/e=360.2 (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 3-picolylamine.
Sources & evidence
- ORD record
- ord-a3d5aa333b644f9cac615f8db8a3a574
- Source dataset
- uspto-grants-2013_03
- Patent number
- US08399674B2
Reaction notes
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