3,5-Dimethylpyrazole → HCID 11848915, compound

HRID 889104Notes

Reaction equation

HRID 889104 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.[Cl:13][C:14]1[CH:20]=[CH:19][C:17]([NH2:18])=[CH:16][CH:15]=1.[CH3:21][C:22]1[CH:26]=[C:25]([CH3:27])[NH:24][N:23]=1>>[Cl:13][C:14]1[CH:20]=[CH:19][C:17]([NH:18][C:10]2[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:3]=[C:2]([N:23]3[C:22]([CH3:21])=[CH:26][C:25]([CH3:27])=[N:24]3)[N:11]=2)=[CH:16][CH:15]=1

Participants

4

Reactant 3

HCID 62103,5-DimethylpyrazoleHCID 78124-ChloroanilineHCID 2528862,4-Dichloroquinazoline

Product 1

HCID 11848915HCID 11848915, compound

Procedure

Was prepared according to Method B from 2,4-dichloroquinazoline, 4-chloroaniline and 3,5-dimethylpyrazole. Mp. 209.3-211.2° C.

Workup

  1. customWas prepared

Sources & evidence

ORD record
ord-afdd3d360c314016986ea765dfabbcc7
Source dataset
uspto-grants-2012_08
Patent number
US08252806B2

Reaction notes

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