2,8-Diacetylamino-1-tetralone → 3-Acetylamino-5-amino-8-methyl-2,3-dihydroquinoline-4-one
Reaction equation
C([N:4]1[C:13]2[C:8](=[C:9]([NH:15]C(=O)C)[CH:10]=[CH:11][C:12]=2[CH3:14])[C:7](=[O:19])[CH:6]([NH:20][C:21](=[O:23])[CH3:22])[CH2:5]1)(=O)C.C(NC1CCC2C(=C(NC(=O)C)C=CC=2)C1=O)(=O)C>>[C:21]([NH:20][CH:6]1[C:7](=[O:19])[C:8]2[C:13](=[C:12]([CH3:14])[CH:11]=[CH:10][C:9]=2[NH2:15])[NH:4][CH2:5]1)(=[O:23])[CH3:22]Participants
3
Procedure
The procedure of Example 1-(4) was followed by using 1.40 gm of the compound prepared in (3) above instead of 2,8-diacetylamino-1-tetralone. The reaction product was post-treated to obtain 0.79 gm of the title compound.
Workup
- additionThe reaction product was post-treated
Sources & evidence
- ORD record
- ord-3780b9bd45e24057b201867d8653291f
- Source dataset
- uspto-grants-2002_06
- Patent number
- US06407115B1
Reaction notes
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