N-(5-Ethyl-2-methyl-indan-2-yl)-benzamide → N-(5,6-diethyl-2-methylindan-2-yl)-benzamide
Reaction equation
[C:1]([C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][C:12]=1[CH2:13][CH3:14])[CH2:9][C:8]([NH:16][C:17](=[O:24])[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)([CH3:15])[CH2:7]2)(=O)[CH3:2].C(C1C=C2C(=CC=1)CC(NC(=O)C1C=CC=CC=1)(C)C2)C>>[CH2:13]([C:12]1[CH:11]=[C:10]2[C:6](=[CH:5][C:4]=1[CH2:1][CH3:2])[CH2:7][C:8]([NH:16][C:17](=[O:24])[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1)([CH3:15])[CH2:9]2)[CH3:14]Participants
3
Procedure
N-(5,6-Diethyl-2-methyl-indan-2-yl)-benzamide is prepared from N-(5-acetyl-6-ethyl-2-methyl-indan-2-yl)-benzamide (1.1 g) following the procedure used to prepare N-(5-ethyl-2-methyl-indan-2-yl)-benzamide. ES+ MS m/e 308 (MH+).
Sources & evidence
- ORD record
- ord-6592ea451dea410e88dc7659f2bfac4d
- Source dataset
- uspto-grants-2009_11
- Patent number
- US07622483B2
Reaction notes
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