3,5-Dimethylpyrazole → HCID 11848971, compound

HRID 889111Notes

Reaction equation

HRID 889111 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.[NH2:13][C:14]1[CH:19]=[CH:18][C:17]([CH3:20])=[CH:16][CH:15]=1.[CH3:21][C:22]1[CH:26]=[C:25]([CH3:27])[NH:24][N:23]=1>>[CH3:21][C:22]1[CH:26]=[C:25]([CH3:27])[N:24]([C:2]2[N:11]=[C:10]([NH:13][C:14]3[CH:19]=[CH:18][C:17]([CH3:20])=[CH:16][CH:15]=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 7813p-ToluidineHCID 2528862,4-Dichloroquinazoline

Product 1

HCID 11848971HCID 11848971, compound

Procedure

Was prepared according to Method B from 2,4-dichloroquinazoline, p-toluidine and 3,5-dimethylpyrazole. Mp. 210.4-216.2° C.

Workup

  1. customWas prepared

Sources & evidence

ORD record
ord-a1b370b6efbc447fac76a7bd39058bb6
Source dataset
uspto-grants-2012_08
Patent number
US08252806B2

Reaction notes

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