3,5-Dimethylpyrazole → HCID 11848917, compound

HRID 889106Notes

Reaction equation

HRID 889106 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][CH:18]=[CH:17][C:15]=1[NH2:16].[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][CH:18]=[CH:17][C:15]=1[NH:16][C:10]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=[C:2]([N:23]2[C:22]([CH3:21])=[CH:26][C:25]([CH3:27])=[N:24]2)[N:11]=1

Participants

4

Reactant 3

HCID 62103,5-DimethylpyrazoleHCID 72402-ChloroanilineHCID 2528862,4-Dichloroquinazoline

Product 1

HCID 11848917HCID 11848917, compound

Procedure

Was prepared according to Method B from 2,4-dichloroquinazoline, 2-chloroaniline and 3,5-dimethylpyrazole. Mp. 210.4-217.1° C.

Workup

  1. customWas prepared

Sources & evidence

ORD record
ord-18df280f94724b94bd4c8977a6762419
Source dataset
uspto-grants-2012_08
Patent number
US08252806B2

Reaction notes

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