HCID 12985698, compound → HCID 23442493, compound
Reaction equation
[Cl:1][C:2]1[C:11]2[C:10](C(C)C)=[CH:9][CH:8]=[CH:7][C:6]=2[N:5]=[C:4]2[CH:15]=[N:16][N:17]([CH3:18])[C:3]=12.[CH:19](C1C2C(=O)C3N(C)N=CC=3NC=2C=CC=1)([CH3:21])[CH3:20].ClC1C2C=CC(F)=CC=2N=C2C=NN(C)C=12.C(C1C=CC2C(=O)C3N(C)N=CC=3NC=2C=1)(C)C>>[Cl:1][C:2]1[C:11]2[CH:10]=[CH:9][C:8]([CH:19]([CH3:21])[CH3:20])=[CH:7][C:6]=2[N:5]=[C:4]2[CH:15]=[N:16][N:17]([CH3:18])[C:3]=12Participants
5
Procedure
A mixture of 9-chloro-8-isopropyl-1-methyl-1H-pyrazolo[4,3-b]quinoline and 9-chloro-6-isopropyl-1-methyl-1H-pyrazolo[4,3-b]quinoline (EXAMPLE 10, step 2) was treated according to the procedure of step 3 in EXAMPLE 3 instead of 9-chloro-6-fluoro-1-methyl-1H-pyrazolo[4,3-b]quinoline. The title compound and 6-isopropyl-1-methyl-1,4-dihydro-9H-pyrazolo[4,3-b]quinolin-9-one were separable by column chromatography on silica gel eluting with methanol/dichloromethane (1:30).
Workup
- additionwas treated
Sources & evidence
- ORD record
- ord-da2f28772ea247488d6cc080cde89347
- Source dataset
- uspto-grants-2004_02
- Patent number
- US06686373B2
Reaction notes
Loading…