HCID 14867574, compound → HCID 14867572, compound
Reaction equation
C1(N2CC3C(=O)N4N=C(C5C=CC(Cl)=CC=5)C=C4N(CC4C=CC=CC=4)C=3C2=O)CCCCC1.[CH:35]1([N:41]2[CH2:49][C:48]3[C:47](=[O:50])[N:46]4[N:51]=[C:52]([C:54]5[CH:59]=[CH:58][C:57](Cl)=[CH:56][CH:55]=5)[CH:53]=[C:45]4[N:44]([CH2:61][C:62](=[O:69])[C:63]4[CH:68]=[CH:67][CH:66]=[CH:65][CH:64]=4)[C:43]=3[C:42]2=[O:70])[CH2:40][CH2:39][CH2:38][CH2:37][CH2:36]1.C(N1CC2C(=O)N3N=C(C4C=CC=CC=4)C=C3N(CC3C=CC=CC=3)C=2C1=O)CCCCC.C(N1CC2C(=O)N3N=C(C4C=CC=CC=4)C=C3N(CC(=O)C3C=CC=CC=3)C=2C1=O)CCCCC.C(N1CC2C(=O)N3N=C(C4C=CC(Cl)=CC=4)C=C3N(CC3C=CC=CC=3)C=2C1=O)CCCCC.C(N1CC2C(=O)N3N=C(C4C=CC(Cl)=CC=4)C=C3N(CC(=O)C3C=CC=CC=3)C=2C1=O)CCCCC>>[CH:35]1([N:41]2[CH2:49][C:48]3[C:47](=[O:50])[N:46]4[N:51]=[C:52]([C:54]5[CH:59]=[CH:58][CH:57]=[CH:56][CH:55]=5)[CH:53]=[C:45]4[N:44]([CH2:61][C:62](=[O:69])[C:63]4[CH:64]=[CH:65][CH:66]=[CH:67][CH:68]=4)[C:43]=3[C:42]2=[O:70])[CH2:36][CH2:37][CH2:38][CH2:39][CH2:40]1Participants
7
Procedure
6-Cyclohexyl-6,7-dihydro-4-(phenylmethyl)-2-(4-chlorophenyl)-4H-pyrazolo[1,5-a]pyrrolo[3,4-d]pyrimidine-5,8-dione; 6-Cyclohexyl-6,7-dihydro-4-(2-oxo-2-phenylethyl)-2-(4-chlorophenyl)-4H-pyrazolo[1,5-a]pyrrolo[3,4-d]-pyrimidine-5,8-dione; 6-Hexyl-6,7-dihydro-4-(phenylmethyl)-2-phenyl-4H- pyrazolo[1,5-a]pyrrolo[3,4-d]-pyrimidine-5,8-dione; 6-Hexyl-6,7-dihydro-4-(2-oxo-2-phenylethyl)-2-phenyl-4H-pyrazolo [1,5-a]-pyrrolo [3,4-d]-pyrimidine-5,8-dione; 6-Hexyl-6,7-dihydro-4-(phenylmethyl)-2-(4-chlorophenyl)-4H-pyrazolo[1,5-a]pyrrolo[3,4-d]-pyrimidine-5,8-dione; 6-Hexyl-6,7-dihydro-4-(2-oxo-2-phenylethyl)-2-(4-chlorophenyl)-4H-pyrazolo[1,5-a]pyrrolo[3,4-d]-pyrimidine-5,8-dione are set forth in Table 15.
Sources & evidence
- ORD record
- ord-2e1389b886784d1ab3d83c9131099697
- Source dataset
- uspto-grants-1996_10
- Patent number
- US05567391
Reaction notes
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