2,8-Diacetylamino-1-tetralone → HCID 22449464, compound
Reaction equation
C(C1CCC2C(=C(C(=O)C)C=CC=2[C:14]#[N:15])C1=O)(=O)C.[C:20]([NH:23][CH:24]1[CH2:33][CH2:32][C:31]2[C:26](=[C:27]([NH:34]C(=O)C)[CH:28]=[CH:29][CH:30]=2)[C:25]1=[O:38])(=[O:22])[CH3:21]>>[C:20]([NH:23][CH:24]1[CH2:33][CH2:32][C:31]2[C:26](=[C:27]([NH2:34])[CH:28]=[CH:29][C:30]=2[C:14]#[N:15])[C:25]1=[O:38])(=[O:22])[CH3:21]Participants
3
Procedure
The reaction was carried out in the same manner as in Example 1-(4), except that 250 mg of the compound prepared in (1) above was used instead of 2,8-diacetylamino-1-tetralone of Example 1-(4), and post-treated to produce 182 mg of the title compound.
Workup
- additionpost-treated
Sources & evidence
- ORD record
- ord-1eaa1e1ed1f648188c77f1611963f83f
- Source dataset
- uspto-grants-2002_06
- Patent number
- US06407115B1
Reaction notes
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