HCID 23442332, compound → HCID 23442337, compound

HRID 2119649Notes

Reaction equation

HRID 2119649 reaction equation
C[O:2][C:3]1[CH:4]=[C:5]([C:9]2[CH:18]=[CH:17][C:16]3[NH:15][C:14]4[CH:19]=[N:20][N:21]([CH3:22])[C:13]=4[C:12](=[O:23])[C:11]=3[CH:10]=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[CH:18]=[CH:17][C:16]3[NH:15][C:14]4[CH:19]=[N:20][N:21]([CH3:22])[C:13]=4[C:12](=[O:23])[C:11]=3[CH:10]=2)[CH:6]=[CH:7][CH:8]=1

Participants

3

Reactant 2

HCID 23442332HCID 23442332, compoundHCID 23442377HCID 23442377, compound

Product 1

HCID 23442337HCID 23442337, compound

Procedure

The title compound was prepared according to the procedure of step 4 in EXAMPLE 38 using 7-(3-methoxyphenyl)-1-methyl-1,4-dihydro-9H-pyrazolo[4,3-b]quinolin-9-one (EXAMPLE 40, 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-c43c2e898742465c8a6132c9fa38f43e
Source dataset
uspto-grants-2004_02
Patent number
US06686373B2

Reaction notes

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