Reaction equation
[OH:1][C:2]1[CH:11]=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:4][CH:3]=1.[N:12]1[CH:17]=[CH:16][C:15](CO)=[CH:14][CH:13]=1.[CH3:20]N(C)CCCO>>[N:12]1[CH:13]=[CH:14][CH:15]=[CH:16][C:17]=1[CH2:20][O:1][C:2]1[CH:3]=[CH:4][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:10][CH:11]=1Participants
4
Procedure
Following the procedure of Example 76(a) except substituting methyl 3-hydroxybenzoate for methyl 4-hydroxybenzoate and 4-pyridylcarbinol for 3-dimethylamino-1-propanol, the title compound was prepared as a yellow solid (0.599 g, 2.5 mmol). MS(ESI): 244.1 (M+H)+.
Sources & evidence
- ORD record
- ord-de65e66e652746a28b7067deb7132af3
- Source dataset
- uspto-grants-2003_05
- Patent number
- US06562842B2
Linked notes
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