Phenylacetyl chloride → HCID 66882827, compound
Reaction equation
[C:1]1([CH2:7][C:8](Cl)=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH:11]1([O:16][C:17]2[CH:18]=[C:19]([C:25](=[O:35])[CH2:26][C:27]3[C:32]([Cl:33])=[CH:31][N:30]=[CH:29][C:28]=3[Cl:34])[CH:20]=[CH:21][C:22]=2[O:23][CH3:24])[CH2:15][CH2:14][CH2:13][CH2:12]1>>[CH:11]1([O:16][C:17]2[CH:18]=[C:19](/[C:25](/[O:35][C:8](=[O:9])[CH2:7][C:1]3[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=3)=[CH:26]/[C:27]3[C:32]([Cl:33])=[CH:31][N:30]=[CH:29][C:28]=3[Cl:34])[CH:20]=[CH:21][C:22]=2[O:23][CH3:24])[CH2:15][CH2:14][CH2:13][CH2:12]1Participants
3
Procedure
The compound was obtained starting from phenyl-acetyl chloride and 1-(3-cyclopentyloxy-4-methoxy-phenyl)-2-(3,5-dichloro-pyridin-4-yl)-ethanone following the procedure of Example 7.
Workup
- customThe compound was obtained
Sources & evidence
- ORD record
- ord-3932e2159624488fa2d57452e7742343
- Source dataset
- uspto-grants-2010_03
- Patent number
- US07671066B2
Reaction notes
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