1-[(3-Chlorophenyl)methyl]-1H-pyrazol-3-amine → 5-[1-(3-Chloro-benzyl)-1H-pyrazol-3-ylamino]-2-(4-methyl-imidazol-1-yl)-benzonitrile

HRID 2063672Notes

Reaction equation

HRID 2063672 reaction equation
Br[C:2]1[CH:3]=[CH:4][C:5]([N:10]2[CH:14]=[C:13]([CH3:15])[N:12]=[CH:11]2)=[C:6]([CH:9]=1)[C:7]#[N:8].[Cl:16][C:17]1[CH:18]=[C:19]([CH:27]=[CH:28][CH:29]=1)[CH2:20][N:21]1[CH:25]=[CH:24][C:23]([NH2:26])=[N:22]1>>[Cl:16][C:17]1[CH:18]=[C:19]([CH:27]=[CH:28][CH:29]=1)[CH2:20][N:21]1[CH:25]=[CH:24][C:23]([NH:26][C:2]2[CH:3]=[CH:4][C:5]([N:10]3[CH:14]=[C:13]([CH3:15])[N:12]=[CH:11]3)=[C:6]([CH:9]=2)[C:7]#[N:8])=[N:22]1

Participants

3

Reactant 2

HCID 161950771-[(3-Chlorophenyl)methyl]-1H-pyrazol-3-amineHCID 669615175-bromo-2-(4-methyl-1H-imidazol-1-yl)benzonitrile

Product 1

HCID 462164175-[1-(3-Chloro-benzyl)-1H-pyrazol-3-ylamino]-2-(4-methyl-imidazol-1-yl)-benzonitrile

Procedure

Prepared in analogy to example 1b) starting with 5-bromo-2-(4-methyl-imidazol-1-yl)-benzonitrile and 1-(3-chloro-benzyl)-1H-pyrazol-3-ylamine. The title compound was obtained as a light yellow solid (Yield=56%). MS ISP (m/e): 389.2 (100) [(M+H)+].

Workup

  1. customPrepared in analogy to example 1b)

Sources & evidence

ORD record
ord-1fd6e5b779f6474d8858b9a42c1f6270
Source dataset
uspto-grants-2012_10
Patent number
US08288403B2

Reaction notes

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