Methoxyacetic Acid → 2-Methoxymethyl-1-phenylmethyl-1H-imidazo[4,5-c]quinoline
Reaction equation
[NH2:1][C:2]1[CH:3]=[N:4][C:5]2[C:10]([C:11]=1[NH:12][CH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)=[CH:9][CH:8]=[CH:7][CH:6]=2.[CH3:20][O:21][CH2:22][C:23](O)=O>>[CH3:20][O:21][CH2:22][C:23]1[N:12]([CH2:13][C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:11]2[C:10]3[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=3[N:4]=[CH:3][C:2]=2[N:1]=1Participants
3
Procedure
Using the general method of Example 91, 3-amino-4-(phenylmethylamino)quinoline (4.0 g, 16 mmol) was reacted with methoxyacetic acid (3.7 mL) to provide 4.4 g of the desired product as a solid. The structure was confirmed by nuclear magnetic resonance spectroscopy.
Sources & evidence
- ORD record
- ord-5d461af6c3484edd8c122a7712728bcd
- Source dataset
- uspto-grants-2002_02
- Patent number
- US06348462B1
Reaction notes
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