1008-79-3 → HCID 66699953, compound
Reaction equation
[CH3:1][C:2]1([CH3:15])[O:11][C:10]2[C:5](=[CH:6][C:7]([C:12]#[N:13])=[CH:8][CH:9]=2)[CH:4]2[O:14][CH:3]12.[C:16]1([N:22]2[CH:26]=[CH:25][C:24](=[O:27])[NH:23]2)[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>>[OH:14][CH:3]1[CH:4]([O:27][C:24]2[CH:25]=[CH:26][N:22]([C:16]3[CH:17]=[CH:18][CH:19]=[CH:20][CH:21]=3)[N:23]=2)[C:5]2[C:10](=[CH:9][CH:8]=[C:7]([C:12]#[N:13])[CH:6]=2)[O:11][C:2]1([CH3:15])[CH3:1]Participants
3
Procedure
Following the procedure in Example 1, using (±)-2,2-dimethyl-1a,7b-dihydro-2H-1,3-dioxa-cyclopropa[a]naphthalene-6-carbonitrile and 1-phenyl-1,2-dihydro-pyrazol-3-one as starting materials, the title compounds were prepared as white solids.
Sources & evidence
- ORD record
- ord-aabd562a90c64e6bb034a66d4858523a
- Source dataset
- uspto-grants-2010_10
- Patent number
- US07812183B2
Reaction notes
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