3,5-Dimethylpyrazole → HCID 131729926, compound

HRID 889095Notes

Reaction equation

HRID 889095 reaction equation
[Cl:1][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][CH:14]([CH2:17][CH3:18])[CH2:15][CH3:16].[CH3:19][C:20]1[CH:24]=[C:23]([CH3:25])[NH:22][N:21]=1>>[ClH:1].[CH3:19][C:20]1[CH:24]=[C:23]([CH3:25])[N:22]([C:2]2[N:11]=[C:10]([NH:13][CH:14]([CH2:17][CH3:18])[CH2:15][CH3:16])[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:3]=2)[N:21]=1

Participants

4

Reactant 3

HCID 62103,5-DimethylpyrazoleHCID 120193-PentanamineHCID 2528862,4-Dichloroquinazoline

Product 1

HCID 131729926HCID 131729926, compound

Procedure

Was prepared according to Method A from 2,4-dichloroquinazoline, 3-aminopentane and 3,5-dimethylpyrazole. Mp. 96.4° C.

Workup

  1. customWas prepared

Sources & evidence

ORD record
ord-0c4938e97cf74142b4f6091c014c81c5
Source dataset
uspto-grants-2012_08
Patent number
US08252806B2

Reaction notes

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