HCID 23442332, compound → HCID 23442394, compound

HRID 2119648Notes

Reaction equation

HRID 2119648 reaction equation
C[O:2][C:3]1[CH:4]=[C:5]([C:9]2[C:10]3[C:11](=[O:23])[C:12]4[N:21]([CH3:22])[N:20]=[CH:19][C:13]=4[NH:14][C:15]=3[CH:16]=[CH:17][CH:18]=2)[CH:6]=[CH:7][CH:8]=1.COC1C=CC(C2C3C(=O)C4N(C)N=CC=4NC=3C=CC=2)=CC=1>>[OH:2][C:3]1[CH:4]=[C:5]([C:9]2[C:10]3[C:11](=[O:23])[C:12]4[N:21]([CH3:22])[N:20]=[CH:19][C:13]=4[NH:14][C:15]=3[CH:16]=[CH:17][CH:18]=2)[CH:6]=[CH:7][CH:8]=1

Participants

3

Reactant 2

HCID 23442332HCID 23442332, compoundHCID 23442406HCID 23442406, compound

Product 1

HCID 23442394HCID 23442394, compound

Procedure

The title compound was prepared according to the procedure of step 4 in EXAMPLE 38 using 8-(3-methoxyphenyl)-1-methyl-1,4-dihydro-9H-pyrazolo[4,3-b]quinolin-9-one (EXAMPLE 39, step 2), instead of 8-(4-methoxyphenyl)-1-methyl-1,4-dihydro-9H-pyrazolo[4,3-b]quinolin-9-one.

Sources & evidence

ORD record
ord-1ebf0e7b97224c28a35ec9200bb52411
Source dataset
uspto-grants-2004_02
Patent number
US06686373B2

Reaction notes

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