HCID 9944890, compound → HCID 9836115, compound
Reaction equation
C[O:2][C:3]1[CH:4]=[C:5]([CH:22]=[CH:23][CH:24]=1)[CH2:6][C:7]1[CH:16]=[CH:15][C:14]2[NH:13][C:12]3[CH:17]=[N:18][N:19]([CH3:20])[C:11]=3[C:10](=[O:21])[C:9]=2[CH:8]=1.COC1C=CC=CC=1CC1C=CC2NC3C=NN(C)C=3C(=O)C=2C=1>>[OH:2][C:3]1[CH:4]=[C:5]([CH:22]=[CH:23][CH:24]=1)[CH2:6][C:7]1[CH:16]=[CH:15][C:14]2[NH:13][C:12]3[CH:17]=[N:18][N:19]([CH3:20])[C:11]=3[C:10](=[O:21])[C:9]=2[CH:8]=1Participants
3
Procedure
The title compound was prepared according to the procedure of step 1 in EXAMPLE 17 using 7-(3-methoxybenzyl)-1-methyl-1,4-dihydro-9H-pyrazolo[4,3-b]quinolin-9-one (EXAMPLE 19, step 4), instead of 7-(2-methoxybenzyl)-1-methyl-1,4-dihydro-9H-pyrazolo[4,3-b]quinolin-9-one.
Sources & evidence
- ORD record
- ord-d0152b65d460464a865cd2f560d95305
- Source dataset
- uspto-grants-2004_02
- Patent number
- US06686373B2
Reaction notes
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