HCID 86649454, compound → 3-[2-(3-Isopropoxy-5-phenoxybenzoylamino)-thiazol-5-yl]-propionic acid ethyl ester
Reaction equation
[CH2:1]([O:3][C:4](=[O:32])[CH:5]=[CH:6][C:7]1[S:11][C:10]([NH:12][C:13](=[O:31])[C:14]2[CH:19]=[C:18]([O:20][C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)[CH:17]=[C:16]([O:27][CH:28]([CH3:30])[CH3:29])[CH:15]=2)=[N:9][CH:8]=1)[CH3:2].[H][H]>CO.[Pd]>[CH2:1]([O:3][C:4](=[O:32])[CH2:5][CH2:6][C:7]1[S:11][C:10]([NH:12][C:13](=[O:31])[C:14]2[CH:19]=[C:18]([O:20][C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=3)[CH:17]=[C:16]([O:27][CH:28]([CH3:29])[CH3:30])[CH:15]=2)=[N:9][CH:8]=1)[CH3:2]Participants
5
Procedure
3-[2-(3-Isopropoxy-5-phenoxybenzoylamino)-thiazol-5-yl]-propionic acid ethyl ester was prepared in 90% yield from the reduction of 3-[2-(3-isopropoxy-5-phenoxybenzoylamino)-thiazol-5-yl]-acrylic acid ethyl ester in methanol (10 mL) using hydrogen (60 psi) over Pd/C (200 mg).
Sources & evidence
- ORD record
- ord-bd6525bba22b4bfeb6d6db971137f552
- Source dataset
- uspto-grants-2012_07
- Patent number
- US08211925B2
Reaction notes
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