3,5-Dimethylpyrazole → HCID 11848920, compound

HRID 889119Notes

Reaction equation

HRID 889119 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:16]=[C:17]([CH:19]=[CH:20][CH:21]=1)[NH2:18].[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:18][C:17]3[CH:19]=[CH:20][CH:21]=[C:15]([C:14]([F:22])([F:23])[F:13])[CH:16]=3)[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:3]=2)[N:26]=1

Participants

4

Procedure

Was prepared according to Method B from 2,4-dichloroquinazoline, 3-trifluoromethylaniline and 3,5-dimethylpyrazole. Mp. 233.1-239.6° C.

Workup

  1. customWas prepared

Sources & evidence

ORD record
ord-8716957902674f2fbacb84bd26afdf6b
Source dataset
uspto-grants-2012_08
Patent number
US08252806B2

Reaction notes

Loading…