N-(2-acetyl-5-methoxyphenyl)-4-Isopropyl-2-Thiazolecarboxamide → N-(6-acetyl-2-fluoro-3-methoxyphenyl)-4-isopropylthiazole-2-carboxamide

HRID 1675400Notes

Reaction equation

HRID 1675400 reaction equation
[NH2:1][C:2]1[C:7]([F:8])=[C:6]([O:9][CH3:10])[CH:5]=[CH:4][C:3]=1[C:11](=[O:13])[CH3:12].[CH:14]([C:17]1[N:18]=[C:19]([C:22](Cl)=[O:23])[S:20][CH:21]=1)([CH3:16])[CH3:15].C(C1C=CC(OC)=CC=1NC(C1SC=C(C(C)C)N=1)=O)(=O)C>>[C:11]([C:3]1[C:2]([NH:1][C:22]([C:19]2[S:20][CH:21]=[C:17]([CH:14]([CH3:16])[CH3:15])[N:18]=2)=[O:23])=[C:7]([F:8])[C:6]([O:9][CH3:10])=[CH:5][CH:4]=1)(=[O:13])[CH3:12]

Participants

4

Reactant 3

HCID 20773655N-(2-acetyl-5-methoxyphenyl)-4-Isopropyl-2-ThiazolecarboxamideHCID 442031471-(2-Amino-3-fluoro-4-methoxyphenyl)ethanoneHCID 575787964-(Propan-2-yl)-1,3-thiazole-2-carbonyl chloride

Product 1

HCID 66650494N-(6-acetyl-2-fluoro-3-methoxyphenyl)-4-isopropylthiazole-2-carboxamideYield 84%

Procedure

Compound 42c was synthesized from 1-(2-amino-3-fluoro-4-methoxyphenyl)ethanone and compound 38 as a beige solid in 84% yield, according to the procedure as described for compound 42a.

Sources & evidence

ORD record
ord-83b1cf73cebc474c9c53254bf7a5bdc9
Source dataset
uspto-grants-2011_08
Patent number
US08003659B2

Reaction notes

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