1-Propanol → Propyl 4-[7-(3-methylisoxazol-5-yl)heptoxy]benzoate
Reaction equation
[C:1]([C:4]1[CH:23]=[CH:22][C:7]([O:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][C:16]2[O:20][N:19]=[C:18]([CH3:21])[CH:17]=2)=[CH:6][CH:5]=1)([OH:3])=[O:2].[CH2:24](O)[CH2:25][CH3:26]>>[CH2:24]([O:2][C:1]([C:4]1[CH:5]=[CH:6][C:7]([O:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][C:16]2[O:20][N:19]=[C:18]([CH3:21])[CH:17]=2)=[CH:22][CH:23]=1)=[O:3])[CH2:25][CH3:26]Participants
3
Procedure
[I; R is CH3, n is 7, X is O, Ar is 4--CH3 (CH2)2OOCC6H4 ], m.p. 54° C., from 5-[7-(4-carboxyphenoxy)heptyl]-3-methylisoxazole (Example 16) and n-propyl alcohol; MIC vs. rhinovirus Type 2 in vitro=0.07 μg/ml.
Sources & evidence
- ORD record
- ord-af0fc335aa43428c9909e138d434cb69
- Source dataset
- uspto-grants-1984_05
- Patent number
- US04451476
Reaction notes
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