3,5-Dimethylpyrazole → HCID 11848972, compound

HRID 889112Notes

Reaction equation

HRID 889112 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]=[C:16]([CH3:20])[CH:15]=1.[CH3:21][C:22]1[CH:26]=[C:25]([CH3:27])[NH:24][N:23]=1>>[CH3:21][C:22]1[CH:26]=[C:25]([CH3:27])[N:24]([C:2]2[N:11]=[C:10]([NH:13][C:14]3[CH:15]=[C:16]([CH3:20])[CH:17]=[CH:18][CH:19]=3)[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:3]=2)[N:23]=1

Participants

4

Reactant 3

HCID 62103,5-DimethylpyrazoleHCID 7934m-ToluidineHCID 2528862,4-Dichloroquinazoline

Product 1

HCID 11848972HCID 11848972, compound

Procedure

Was prepared according to Method B from 2,4-dichloroquinazoline, m-toluidine and 3,5-dimethylpyrazole. Mp. 249.2-250.4° C.

Workup

  1. customWas prepared

Sources & evidence

ORD record
ord-9747bd77f2a946a7a15a2f9eab9ebeb4
Source dataset
uspto-grants-2012_08
Patent number
US08252806B2

Reaction notes

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