3-Phenylpropylamine → Ethyl 5-{[(3-phenylpropyl)amino]methyl}-2-furoate
Reaction equation
[CH:1]([C:3]1[O:7][C:6]([C:8]([O:10][CH2:11][CH3:12])=[O:9])=[CH:5][CH:4]=1)=O.[C:13]1([CH2:19][CH2:20][CH2:21][NH2:22])[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1>>[C:13]1([CH2:19][CH2:20][CH2:21][NH:22][CH2:1][C:3]2[O:7][C:6]([C:8]([O:10][CH2:11][CH3:12])=[O:9])=[CH:5][CH:4]=2)[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1Participants
3
Procedure
Subsequently, ethyl 5-{[(3-phenylpropyl)amino]methyl}-2-furoate (0.64 g) was prepared from ethyl 5-formyl-furan-2-carboxylate (500 mg) and 3-phenylpropylamine (0.85 mL) in the same manner as in Preparation Example 52.
Sources & evidence
- ORD record
- ord-987e812ee7ee4061a3f30a6e7e7f5f78
- Source dataset
- uspto-grants-2014_03
- Patent number
- US08669246B2
Reaction notes
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