Isopropanol → HCID 11619106, compound

HRID 2104152Notes

Reaction equation

HRID 2104152 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([O:8][C:9]([F:12])([F:11])[F:10])=[CH:4][C:3]=1[C:13]([C:15]1[CH:20]=[CH:19][CH:18]=[C:17]([Cl:21])[CH:16]=1)=O.[C:22]([CH2:30][C:31](=O)[CH3:32])(=[O:29])[C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1.C(O)(C)C>CCCCCCC.C(OCC)(=O)C>[Cl:21][C:17]1[CH:16]=[C:15]([C:13]2[C:3]3[C:2](=[CH:7][CH:6]=[C:5]([O:8][C:9]([F:12])([F:11])[F:10])[CH:4]=3)[N:1]=[C:31]([CH3:32])[C:30]=2[C:22]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=2)=[O:29])[CH:20]=[CH:19][CH:18]=1

Participants

5

Reactant 3

HCID 3776IsopropanolHCID 7166BenzoylacetoneHCID 67549809HCID 67549809, compound

Product 1

HCID 11619106HCID 11619106, compoundYield 57%

Reagents, catalysts & solvents 1

HCID 21899848Ethylacetate heptaneSolvent

Procedure

The title compound was prepared from (2-Amino-5-trifluoromethoxy-phenyl)-(3-chloro-phenyl)-methanone [example A7] and benzoylacetone according to the procedure of example 1, except that the solvent was isopropanol, and heptane/ethyl acetate (1:2) was used. Yield: 57%; MS: m/z=441 (M).

Sources & evidence

ORD record
ord-b9cc0a8aa8ab4756ac2825e26eb8d4e0
Source dataset
uspto-grants-2009_08
Patent number
US07576217B2

Reaction notes

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