1-Isopropylhydrazine hydrochloride → 5-(5-chloro-1-methyl-6-oxo-1,6-dihydropyridin-3-yl)-4-(4-chlorophenyl)-1-isopropyl-3-methyl-4,5-dihydropyrrolo-[3,4-c]pyrazol-6(1H)-one
Reaction equation
[C:1]([C:4]1[CH:5]([C:20]2[CH:25]=[CH:24][C:23]([Cl:26])=[CH:22][CH:21]=2)[N:6]([C:11]2[CH:12]=[C:13]([Cl:19])[C:14](=[O:18])[N:15]([CH3:17])[CH:16]=2)[C:7](=[O:10])[C:8]=1O)(=O)[CH3:2].Cl.[CH:28]([NH:31][NH2:32])([CH3:30])[CH3:29]>CCOC(C)=O>[Cl:19][C:13]1[C:14](=[O:18])[N:15]([CH3:17])[CH:16]=[C:11]([N:6]2[CH:5]([C:20]3[CH:21]=[CH:22][C:23]([Cl:26])=[CH:24][CH:25]=3)[C:4]3[C:1]([CH3:2])=[N:32][N:31]([CH:28]([CH3:30])[CH3:29])[C:8]=3[C:7]2=[O:10])[CH:12]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The title compound was prepared in analogy to the procedure described in Example 58 using 5-(3-acetyl-2-(4-chlorophenyl)-4-hydroxy-5-oxo-2,5-dihydro-1H-pyrrol-1-yl)-3-chloro-1-methyl-pyridin-2(1H)-one (Step 58.1) and isopropylhydrazine hydrochloride. tR: 4.69 min (HPLC 1); tR: 1.09 min (LC-MS 2); ESI-MS: 431/433 [M+H]+ (LC-MS 2); Rf=0.55 (EtOAc); 1H NMR (400 MHz, DMSO-d6) δ ppm 1.45-1.57 (m, 6H) 1.93 (s, 3H) 3.44 (s, 3H) 4.67-4.79 (m, 1H) 6.11 (s, 1H) 7.28 (d, J=8.2 Hz, 2H) 7.40 (d, J=8.2 Hz, 2H) 7.91 (d, J=2.0 Hz, 1H) 7.95 (d, J=2.4 Hz, 1H).
Sources & evidence
- ORD record
- ord-2bb9a5f79cf243aeacc2ae55c41d898b
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08975417B2
Reaction notes
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