HCID 23442326, compound → HCID 23442477, compound

HRID 2119643Notes

Reaction equation

HRID 2119643 reaction equation
[CH3:1][N:2]1[C:14]2[C:13](=[O:15])[C:12]3[CH:11]=[C:10]([CH2:16][C:17]4[CH:24]=[CH:23][CH:22]=[CH:21][C:18]=4[C:19]#[N:20])[CH:9]=[CH:8][C:7]=3[NH:6][C:5]=2[CH:4]=[N:3]1.CN1C2C(=[O:39])C3C=C(CC4C=C(C=CC=4)C#N)C=CC=3NC=2C=N1>>[CH3:1][N:2]1[C:14]2[C:13](=[O:15])[C:12]3[CH:11]=[C:10]([CH2:16][C:17]4[CH:24]=[CH:23][CH:22]=[CH:21][C:18]=4[C:19]([NH2:20])=[O:39])[CH:9]=[CH:8][C:7]=3[NH:6][C:5]=2[CH:4]=[N:3]1

Participants

3

Reactant 2

HCID 23442326HCID 23442326, compoundHCID 23442359HCID 23442359, compound

Product 1

HCID 23442477HCID 23442477, compound

Procedure

The title compound was prepared according to the procedure of EXAMPLE 29 using 2-[(1-methyl-9-oxo-4,9-dihydro-1H-pyrazolo[4,3-b]quinolin-7-yl)methyl]benzonitrile (EXAMPLE 32, step 2), instead of 3-[(1-methyl-9-oxo-4,9-dihydro-1H-pyrazolo[4,3-b]quinolin-7-yl)methyl]benzonitrile.

Sources & evidence

ORD record
ord-94c306edeb844398aa0a47a2e00438fd
Source dataset
uspto-grants-2004_02
Patent number
US06686373B2

Reaction notes

Loading…