HCID 12985697, compound → HCID 23442370, compound

HRID 2119622Notes

Reaction equation

HRID 2119622 reaction equation
[CH:1]([C:4]1[CH:5]=[C:6]([NH:10][C:11]2[CH:12]=[N:13][N:14]([CH3:19])[C:15]=2[C:16]([OH:18])=O)[CH:7]=[CH:8][CH:9]=1)([CH3:3])[CH3:2].FC1C=C(NC2C=NN(C)C=2C(O)=O)C=CC=1>>[CH:1]([C:4]1[C:5]2[C:16](=[O:18])[C:15]3[N:14]([CH3:19])[N:13]=[CH:12][C:11]=3[NH:10][C:6]=2[CH:7]=[CH:8][CH:9]=1)([CH3:2])[CH3:3]

Participants

3

Reactant 2

HCID 12985697HCID 12985697, compoundHCID 23442330HCID 23442330, compound

Product 1

HCID 23442370HCID 23442370, compound

Procedure

The title compounds were prepared as an inseparable mixture with a ratio of 1.2:3 according to the procedure of step 2 in EXAMPLE 3 using 4-[(3-isopropylphenyl)amino]-1-methyl-1H-pyrazole-5-carboxylic acid (EXAMPLE 10, step 1), instead of 4-[(3-fluorophenyl)amino]-1-methyl-1H-pyrazole-5-carboxylic acid.

Sources & evidence

ORD record
ord-5dc782e266e24c1da26fed309b2dafb4
Source dataset
uspto-grants-2004_02
Patent number
US06686373B2

Reaction notes

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