4-Methoxy-3-methylbenzoic Acid → (r/s)-4-Methoxy-n-(5-methoxy-2,3-dihydro-1h-inden-1-yl)-3-methylbenzamide
Reaction equation
[CH3:1][O:2][C:3]1[CH:11]=[CH:10][C:6]([C:7]([OH:9])=O)=[CH:5][C:4]=1[CH3:12].[CH3:13][O:14][C:15]1[CH:16]=[C:17]2[C:21](=[CH:22][CH:23]=1)[CH:20]([NH2:24])[CH2:19][CH2:18]2>>[CH3:1][O:2][C:3]1[CH:11]=[CH:10][C:6]([C:7]([NH:24][CH:20]2[C:21]3[C:17](=[CH:16][C:15]([O:14][CH3:13])=[CH:23][CH:22]=3)[CH2:18][CH2:19]2)=[O:9])=[CH:5][C:4]=1[CH3:12]Participants
3
Procedure
Prepared in a similar manner to example 4 using 4-methoxy-3-methylbenzoic acid and 5-methoxy-2,3-dihydro-1H-inden-1-amine (Example 121-2a) (47%). MS (M+Hs 312).
Sources & evidence
- ORD record
- ord-3b043960374a45b8be6010595d6a1d11
- Source dataset
- uspto-grants-2012_11
- Patent number
- US08318947B2
Reaction notes
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