n-(6-Acetyl-3-chloro-4-methoxyphenyl)-4-isopropylthiazole-2-carboxamide → HCID 178486752, compound
Reaction equation
[C:1]([C:4]1[C:9]([NH:10][C:11]([C:13]2[S:14][CH:15]=[C:16]([CH:18]([CH3:20])[CH3:19])[N:17]=2)=O)=[CH:8][C:7]([Cl:21])=[C:6]([O:22][CH3:23])[CH:5]=1)(=[O:3])[CH3:2].C(C1N=C(C2C=C(O)C3C(=CC(OC)=CC=3)N=2)SC=1)(C)C>>[Cl:21][C:7]1[CH:8]=[C:9]2[C:4]([C:1]([OH:3])=[CH:2][C:11]([C:13]3[S:14][CH:15]=[C:16]([CH:18]([CH3:20])[CH3:19])[N:17]=3)=[N:10]2)=[CH:5][C:6]=1[O:22][CH3:23]Participants
3
Procedure
Compound 43g was synthesized from compound 42g as a yellow solid in 70% yield, according to the procedures as described for compound 43a.
Sources & evidence
- ORD record
- ord-97f0df07ff5147189d6de85fead452d8
- Source dataset
- uspto-grants-2012_01
- Patent number
- US08093379B2
Reaction notes
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