3,5-Dimethylpyrazole → HCID 11849150, compound

HRID 889118Notes

Reaction equation

HRID 889118 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][C:17]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)=[CH:16][CH:15]=1.[CH3:26][C:27]1[CH:31]=[C:30]([CH3:32])[NH:29][N:28]=1>>[C:17]1([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[CH:16]=[CH:15][C:14]([NH:13][C:10]2[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:3]=[C:2]([N:28]3[C:27]([CH3:26])=[CH:31][C:30]([CH3:32])=[N:29]3)[N:11]=2)=[CH:19][CH:18]=1

Participants

4

Procedure

Was prepared according to Method B from 2,4-dichloroquinazoline, 4-aminobiphenyl and 3,5-dimethylpyrazole. Mp. 267.5-270.3° C.

Workup

  1. customWas prepared

Sources & evidence

ORD record
ord-0a43edb192b941daa6be5e020f46d22e
Source dataset
uspto-grants-2012_08
Patent number
US08252806B2

Reaction notes

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