Methyl 2-(2-hydroxyethyl)-4,5,6,7-tetrahydronaphtho[2,1-b]furan-7-carboxylate → 2-(2-(3-Phenyl-7-propylbenz[4,5]isoxazol-6-yloxy)ethyl)-4,5,6,7-tetrahydronaphtho[2,1-b]furan-7-carboxylic acid
Reaction equation
[OH:1][CH2:2][CH2:3][C:4]1[O:8][C:7]2[CH2:9][CH2:10][C:11]3[CH2:12][CH:13]([C:17]([O:19]C)=[O:18])[CH:14]=[CH:15][C:16]=3[C:6]=2[CH:5]=1.[C:21]1([C:27]2[C:31]3[CH:32]=[CH:33][C:34](O)=[C:35]([CH2:36][CH2:37][CH3:38])[C:30]=3[O:29][N:28]=2)[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1>>[C:21]1([C:27]2[C:31]3[CH:32]=[CH:33][C:34]([O:1][CH2:2][CH2:3][C:4]4[O:8][C:7]5[CH2:9][CH2:10][C:11]6[CH2:12][CH:13]([C:17]([OH:19])=[O:18])[CH:14]=[CH:15][C:16]=6[C:6]=5[CH:5]=4)=[C:35]([CH2:36][CH2:37][CH3:38])[C:30]=3[O:29][N:28]=2)[CH:22]=[CH:23][CH:24]=[CH:25][CH:26]=1Participants
3
Procedure
Using the procedure from Example 1, steps F and G, the title compound was prepared from methyl 2-(2-hydroxyethyl)-4,5,6,7-tetrahydronaphtho[2,1-b]furan-7-carboxylate and 3-phenyl-7-propyl-6-hydroxybenz[4,5]isoxazole as a colorless oil.
Sources & evidence
- ORD record
- ord-c742d7ba25c34ca68def3e2379ecdf6e
- Source dataset
- uspto-grants-2000_07
- Patent number
- US06090839
Reaction notes
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