HCID 15083504, compound → HCID 86617864, compound

HRID 2242073Notes

Reaction equation

HRID 2242073 reaction equation
[C:1]1([CH3:13])[CH:6]=[CH:5][C:4]([C:7]2([C:10](Cl)=[O:11])[CH2:9][CH2:8]2)=[CH:3][CH:2]=1.[Cl:14][C:15]1[CH:16]=[N:17][CH:18]=[C:19]([Cl:34])[C:20]=1[CH2:21][C:22]([C:24]1[CH:29]=[CH:28][C:27]([O:30][CH3:31])=[C:26]([O:32][CH3:33])[CH:25]=1)=[O:23]>>[C:1]1([CH3:13])[CH:6]=[CH:5][C:4]([C:7]2([C:10]([O:23]/[C:22](/[C:24]3[CH:29]=[CH:28][C:27]([O:30][CH3:31])=[C:26]([O:32][CH3:33])[CH:25]=3)=[CH:21]\[C:20]3[C:19]([Cl:34])=[CH:18][N:17]=[CH:16][C:15]=3[Cl:14])=[O:11])[CH2:9][CH2:8]2)=[CH:3][CH:2]=1

Participants

3

Procedure

The compound was obtained starting from 1-p-tolyl-cyclopropanecarbonyl chloride and 2-(3,5-dichloro-pyridin-4-yl)-1-(3,4-dimethoxy -phenyl)-ethanone, following the procedure of Example 7.

Workup

  1. customThe compound was obtained

Sources & evidence

ORD record
ord-5c1716d918a74370ae5567fdc2e5975c
Source dataset
uspto-grants-2010_03
Patent number
US07671066B2

Reaction notes

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