4-Pyridinemethanamine → HCID 68574453, 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][C:14]1[O:18][C:17]([CH2:19][NH2:20])=[CH:16][CH:15]=1.[NH2:21][CH2:22][C:23]1[CH:28]=[CH:27][N:26]=[CH:25][CH:24]=1>>[CH3:13][C:14]1[O:18][C:17]([CH2:19][NH:20][C:2]2[CH:11]=[CH:10][C:9]3[C:4](=[CH:5][CH:6]=[C:7]([NH:21][CH2:22][C:23]4[CH:28]=[CH:27][N:26]=[CH:25][CH:24]=4)[CH:8]=3)[N:3]=2)=[CH:16][CH:15]=1Participants
4
Procedure
The title compound, MS: m/e=345.1 (M+H+), was prepared in accordance with the general method of example 1 from 2,6-dichloroquinoline, 5-methyl-2-furanmethanamine and 4-(aminomethyl)pyridine.
Sources & evidence
- ORD record
- ord-69e15ddc9bc94eb99830b589ef7618ea
- Source dataset
- uspto-grants-2013_03
- Patent number
- US08399674B2
Reaction notes
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