3,5-Dimethylpyrazole → HCID 131729928, compound

HRID 889097Notes

Reaction equation

HRID 889097 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.[CH3:13][CH:14]1[CH2:19][CH2:18][CH:17]([NH2:20])[CH2:16][CH2:15]1.[CH3:21][C:22]1[CH:26]=[C:25]([CH3:27])[NH:24][N:23]=1>>[ClH:1].[CH3:21][C:22]1[CH:26]=[C:25]([CH3:27])[N:24]([C:2]2[N:11]=[C:10]([NH:20][CH:17]3[CH2:18][CH2:19][CH:14]([CH3:13])[CH2:15][CH2:16]3)[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:3]=2)[N:23]=1

Participants

4

Reactant 3

HCID 62103,5-DimethylpyrazoleHCID 806044-MethylcyclohexylamineHCID 2528862,4-Dichloroquinazoline

Product 1

HCID 131729928HCID 131729928, compound

Procedure

Was prepared according to Method A from 2,4-dichloroquinazoline, 4-methylcyclohexylamine and 3,5-dimethylpyrazole. Mp. 80.4-81.6° C.

Workup

  1. customWas prepared

Sources & evidence

ORD record
ord-2bddddc99cf24151b70bc57f1ba24618
Source dataset
uspto-grants-2012_08
Patent number
US08252806B2

Reaction notes

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