2-Aminomethylquinoline → HCID 10132107, compound

HRID 1356034

Reaction equation

HRID 1356034 reaction equation
[NH2:1][C:2]1[N:7]=[C:6]([C:8]2[O:9][CH:10]=[CH:11][CH:12]=2)[C:5]([C:13]#[N:14])=[C:4](OS(C(F)(F)F)(=O)=O)[CH:3]=1.[NH2:23][CH2:24][C:25]1[CH:34]=[CH:33][C:32]2[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=2)[N:26]=1>COCCOC>[NH2:1][C:2]1[CH:3]=[C:4]([NH:23][CH2:24][C:25]2[CH:34]=[CH:33][C:32]3[C:27](=[CH:28][CH:29]=[CH:30][CH:31]=3)[N:26]=2)[C:5]([C:13]#[N:14])=[C:6]([C:8]2[O:9][CH:10]=[CH:11][CH:12]=2)[N:7]=1

Participants

4

Reactant 2

HCID 30143782-AminomethylquinolineHCID 86583754HCID 86583754, compound

Product 1

HCID 10132107HCID 10132107, compound

Reagents, catalysts & solvents 1

HCID 80711,2-DimethoxyethaneSolvent

Procedure

From trifluoromethanesulfonic acid 6-amino-3-cyano-2-furan-2-yl-pyridin-4-yl ester and 2-(aminomethyl)quinoline in DME. ES-MS m/e (%): 342 (M+H+, 100).

Sources & evidence

ORD record
ord-1228e7b16ac947da8049e41440d813b5
Source dataset
uspto-grants-2003_07
Patent number
US06586441B2

Linked notes

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