3,5-Dimethylpyrazole → HCID 11849030, compound

HRID 889120Notes

Reaction equation

HRID 889120 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.[NH2:13][C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][N:15]=1.[CH3:20][C:21]1[CH:25]=[C:24]([CH3:26])[NH:23][N:22]=1>>[CH3:20][C:21]1[CH:25]=[C:24]([CH3:26])[N:23]([C:2]2[N:11]=[C:10]([NH:13][C:14]3[CH:19]=[CH:18][CH:17]=[CH:16][N:15]=3)[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:3]=2)[N:22]=1

Participants

4

Reactant 3

HCID 62103,5-DimethylpyrazoleHCID 104392-AminopyridineHCID 2528862,4-Dichloroquinazoline

Product 1

HCID 11849030HCID 11849030, compound

Procedure

Was prepared according to Method B from 2,4-dichloroquinazoline, 2-aminopyridine and 3,5-dimethylpyrazole. Mp. 126.1-126.8° C.

Workup

  1. customWas prepared

Sources & evidence

ORD record
ord-eac604fa2d1f4ecc99ca17c960397361
Source dataset
uspto-grants-2012_08
Patent number
US08252806B2

Reaction notes

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