3,5-Dimethylpyrazole → HCID 11848919, compound

HRID 889108Notes

Reaction equation

HRID 889108 reaction equation
Cl[C:2]1[N:11]=[C:10](Cl)[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=1.[Br:13][C:14]1[CH:20]=[CH:19][C:17]([NH2:18])=[CH:16][CH:15]=1.[CH3:21][C:22]1[CH:26]=[C:25]([CH3:27])[NH:24][N:23]=1>>[Br:13][C:14]1[CH:20]=[CH:19][C:17]([NH:18][C:10]2[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:3]=[C:2]([N:23]3[C:22]([CH3:21])=[CH:26][C:25]([CH3:27])=[N:24]3)[N:11]=2)=[CH:16][CH:15]=1

Participants

4

Reactant 3

HCID 62103,5-DimethylpyrazoleHCID 78074-BromoanilineHCID 2528862,4-Dichloroquinazoline

Product 1

HCID 11848919HCID 11848919, compound

Procedure

Was prepared according to Method B from 2,4-dichloroquinazoline, 4-bromoaniline and 3,5-dimethylpyrazole. Mp. 116.2-168.3° C.

Workup

  1. customWas prepared

Sources & evidence

ORD record
ord-0be93d515a524ea7ace107051e177866
Source dataset
uspto-grants-2012_08
Patent number
US08252806B2

Reaction notes

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