3,5-Dimethylpyrazole → HCID 131729921, compound

HRID 889090Notes

Reaction equation

HRID 889090 reaction equation
[Cl:1][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.[CH2:13]([NH2:20])[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1.[CH3:21][C:22]1[CH:26]=[C:25]([CH3:27])[NH:24][N:23]=1>>[ClH:1].[CH2:13]([NH:20][C:10]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=[C:2]([N:23]2[C:22]([CH3:21])=[CH:26][C:25]([CH3:27])=[N:24]2)[N:11]=1)[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1

Participants

4

Procedure

Was prepared according to Method A from 2,4-dichloroquinazoline, benzylamine and 3,5-dimethylpyrazole. Mp. 160.2° C.

Workup

  1. customWas prepared

Sources & evidence

ORD record
ord-c2246ba5804a4720955f79c5d26a84a0
Source dataset
uspto-grants-2012_08
Patent number
US08252806B2

Reaction notes

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