4-(4-chloro-2-fluorophenyl)-5-(3,8-dimethyl-[1,2,4]triazolo[4,3-a]pyridin-6-yl)-1-isopropyl-3-methyl-4,5-dihydropyrrolo[3,4-c]pyrazol-6(1H)-one → (S)-4-(4-chloro-2-fluorophenyl)-5-(3,8-dimethyl-[1,2,4]triazolo[4,3-a]pyridin-6-yl)-1-isopropyl-3-methyl-4,5-dihydropyrrolo[3,4-c]pyrazol-6(1H)-one
Reaction equation
ClC1C=CC(C2C3C(C)=NN(C4CN(C(OC(C)(C)C)=O)C4)C=3C(=O)N2C2C=C(C)C3N(C(C)=NN=3)C=2)=CC=1.[Cl:40][C:41]1[CH:46]=[CH:45][C:44]([CH:47]2[C:54]3[C:53]([CH3:55])=[N:52][N:51]([CH:56]([CH3:58])[CH3:57])[C:50]=3[C:49](=[O:59])[N:48]2[C:60]2[CH:61]=[C:62]([CH3:70])[C:63]3[N:64]([C:66]([CH3:69])=[N:67][N:68]=3)[CH:65]=2)=[C:43]([F:71])[CH:42]=1>CC(O)C>[Cl:40][C:41]1[CH:46]=[CH:45][C:44]([C@@H:47]2[C:54]3[C:53]([CH3:55])=[N:52][N:51]([CH:56]([CH3:58])[CH3:57])[C:50]=3[C:49](=[O:59])[N:48]2[C:60]2[CH:61]=[C:62]([CH3:70])[C:63]3[N:64]([C:66]([CH3:69])=[N:67][N:68]=3)[CH:65]=2)=[C:43]([F:71])[CH:42]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound (65 mg, 43% yield) was obtained enantiomerically pure (>99% ee) after chiral preparative chromatography (system: MGII preparative SFC; column: Chiralpak AD-H, 30×250 mm; mobile phase: scCO2/iPrOH 75:25; flow: 50 mL/min; temperature: 38° C.; detection UV: 220 nm) of the racemic mixture of 4-(4-chloro-2-fluorophenyl)-5-(3,8-dimethyl-[1,2,4]triazolo[4,3-a]pyridin-6-yl)-1-isopropyl-3-methyl-4,5-dihydropyrrolo[3,4-c]pyrazol-6(1H)-one (Example 168).
Sources & evidence
- ORD record
- ord-e2271dbe1ac94c06a603f610ff2112b5
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08975417B2
Reaction notes
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