5-[1-(6-Methoxy-2-naphthyl)ethyl]-2-phenyl-4-hydroxythiazole → 5-[1-(6-Methoxy-2-naphthyl)ethyl]-2-phenyl-4-methoxycarbonyloxythiazole
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[C:8]([CH:13]([C:15]1[S:19][C:18]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)=[N:17][C:16]=1[OH:26])[CH3:14])[CH:7]=[CH:6]2.Cl[CH2:28][O:29][CH:30]=[O:31]>N1C=CC=CC=1>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[CH:9]=[C:8]([CH:13]([C:15]1[S:19][C:18]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)=[N:17][C:16]=1[O:26][C:30]([O:29][CH3:28])=[O:31])[CH3:14])[CH:7]=[CH:6]2Participants
4
Procedure
The desired compound is prepared by treatment of the product of Example 5 with chloromethylformate and pyridine.
Sources & evidence
- ORD record
- ord-541f6c4a5bf14fb9b40f0353f8d71e69
- Source dataset
- uspto-grants-1991_07
- Patent number
- US05032588
Reaction notes
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