3,5-Dimethylpyrazole → HCID 11848969, compound

HRID 889109Notes

Reaction equation

HRID 889109 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.[F:13][C:14]([F:23])([F:22])[C:15]1[CH:21]=[CH:20][C:18]([NH2:19])=[CH:17][CH:16]=1.[CH3:24][C:25]1[CH:29]=[C:28]([CH3:30])[NH:27][N:26]=1>>[CH3:24][C:25]1[CH:29]=[C:28]([CH3:30])[N:27]([C:2]2[N:11]=[C:10]([NH:19][C:18]3[CH:20]=[CH:21][C:15]([C:14]([F:22])([F:23])[F:13])=[CH:16][CH:17]=3)[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:3]=2)[N:26]=1

Participants

4

Reactant 3

HCID 62103,5-DimethylpyrazoleHCID 99644-(Trifluoromethyl)anilineHCID 2528862,4-Dichloroquinazoline

Product 1

HCID 11848969HCID 11848969, compound

Procedure

Was prepared according to Method B from 2,4-dichloroquinazoline, 4-trifluoromethylaniline and 3,5-dimethylpyrazole. Mp. 218.8-220.1° C.

Workup

  1. customWas prepared

Sources & evidence

ORD record
ord-9fc273206e9f40a1a072961104394013
Source dataset
uspto-grants-2012_08
Patent number
US08252806B2

Reaction notes

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