3,5-Dimethylpyrazole → HCID 131729922, compound

HRID 889091Notes

Reaction equation

HRID 889091 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.[Cl:13][C:14]1[CH:21]=[CH:20][C:17]([CH2:18][NH2:19])=[CH:16][CH:15]=1.[CH3:22][C:23]1[CH:27]=[C:26]([CH3:28])[NH:25][N:24]=1>>[ClH:1].[Cl:13][C:14]1[CH:21]=[CH:20][C:17]([CH2:18][NH:19][C:10]2[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:3]=[C:2]([N:24]3[C:23]([CH3:22])=[CH:27][C:26]([CH3:28])=[N:25]3)[N:11]=2)=[CH:16][CH:15]=1

Participants

4

Reactant 3

HCID 62103,5-DimethylpyrazoleHCID 660364-ChlorobenzylamineHCID 2528862,4-Dichloroquinazoline

Product 1

HCID 131729922HCID 131729922, compound

Procedure

Was prepared according to Method A from 2,4-dichloroquinazoline, 4-chlorobenzylamine and 3,5-dimethylpyrazole. LC-ESI-HRMS [M+H]+ 364.1319 Da. Calc. 364.132898 Da.

Workup

  1. customWas prepared

Sources & evidence

ORD record
ord-1b9f52e78d8e4d848c6f2ae4db311040
Source dataset
uspto-grants-2012_08
Patent number
US08252806B2

Reaction notes

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