HCID 66687731, compound → 1-[5-(3-Bromo-5-methoxy-phenyl)-1-(3-pyridyl)pyrazole-3-carbonyl]imidazolidin-4-one

HRID 930098Notes

Reaction equation

HRID 930098 reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([C:10]2[N:14]([C:15]3[CH:16]=[N:17][CH:18]=[CH:19][CH:20]=3)[N:13]=[C:12]([C:21]([OH:23])=O)[CH:11]=2)[CH:5]=[C:6]([O:8][CH3:9])[CH:7]=1.ClC1C=C(C2N(C3C=CC=CN=3)N=C(C([N:45]3[CH2:49][C:48](=[O:50])[NH:47][CH2:46]3)=O)C=2)C=C(F)C=1.Cl.N1C=CNC1=O>>[Br:1][C:2]1[CH:3]=[C:4]([C:10]2[N:14]([C:15]3[CH:16]=[N:17][CH:18]=[CH:19][CH:20]=3)[N:13]=[C:12]([C:21]([N:45]3[CH2:49][C:48](=[O:50])[NH:47][CH2:46]3)=[O:23])[CH:11]=2)[CH:5]=[C:6]([O:8][CH3:9])[CH:7]=1

Participants

4

Reactant 3

HCID 66687731HCID 66687731, compoundHCID 71576484HCID 71576484, compoundHCID 896025285-(3-Bromo-5-methoxyphenyl)-1-(pyridin-3-yl)-1H-pyrazole-3-carboxylic acid

Product 1

HCID 715665471-[5-(3-Bromo-5-methoxy-phenyl)-1-(3-pyridyl)pyrazole-3-carbonyl]imidazolidin-4-one

Procedure

80 mg (0.21 mmol) of the compound of Example 50A is reacted analogously to the synthesis of the compound of Example 1 with 29 mg (0.24 mmol) of 4-imidazolinone-hydrochloride. 76 mg (79% of theory) of the title compound is obtained.

Sources & evidence

ORD record
ord-6e8213328f304e9fadd6d249dda07e62
Source dataset
uspto-grants-2016_03
Patent number
US09296720B2

Reaction notes

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