4-(2,5-Dimethyl-1H-pyrrol-1-yl)benzaldehyde → HCID 58762772, compound
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([CH2:10][CH2:11][C:12]2([CH:20]3[CH2:24][CH2:23][CH2:22][CH2:21]3)[O:17][C:16](=[O:18])[CH2:15][C:14](=[O:19])[CH2:13]2)[CH:5]=[CH:6][C:7]=1[O:8][CH3:9].[CH3:25][C:26]1[N:27]([C:32]2[CH:39]=[CH:38][C:35]([CH:36]=O)=[CH:34][CH:33]=2)[C:28]([CH3:31])=[CH:29][CH:30]=1>>[Cl:1][C:2]1[CH:3]=[C:4]([CH2:10][CH2:11][C:12]2([CH:20]3[CH2:24][CH2:23][CH2:22][CH2:21]3)[O:17][C:16](=[O:18])[C:15]([CH2:36][C:35]3[CH:34]=[CH:33][C:32]([N:27]4[C:28]([CH3:31])=[CH:29][CH:30]=[C:26]4[CH3:25])=[CH:39][CH:38]=3)=[C:14]([OH:19])[CH2:13]2)[CH:5]=[CH:6][C:7]=1[O:8][CH3:9]Participants
3
Procedure
The title compound was prepared by coupling 6-[2-(3-Chloro-4-methoxy-phenyl)-ethyl]-6-cyclopentyl-dihydro-pyran-2,4-dione to 4-(2,5-Dimethyl-pyrrol-1-yl)-benzaldehyde using the Me2NHBH3 method described in the synthesis of Example B(31).
Sources & evidence
- ORD record
- ord-f4e21b569c6b47918fd28e1fd0b992c8
- Source dataset
- uspto-grants-2006_12
- Patent number
- US07148226B2
Reaction notes
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