3,5-Dimethylpyrazole → HCID 11849089, compound

HRID 889116Notes

Reaction equation

HRID 889116 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]([N:20]2[CH2:25][CH2:24][O:23][CH2:22][CH2:21]2)=[CH:16][CH:15]=1.[CH3:26][C:27]1[CH:31]=[C:30]([CH3:32])[NH:29][N:28]=1>>[CH3:26][C:27]1[CH:31]=[C:30]([CH3:32])[N:29]([C:2]2[N:11]=[C:10]([NH:13][C:14]3[CH:15]=[CH:16][C:17]([N:20]4[CH2:25][CH2:24][O:23][CH2:22][CH2:21]4)=[CH:18][CH:19]=3)[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:3]=2)[N:28]=1

Participants

4

Reactant 3

HCID 62103,5-DimethylpyrazoleHCID 75655Benzenamine, 4-(4-morpholinyl)-HCID 2528862,4-Dichloroquinazoline

Product 1

HCID 11849089HCID 11849089, compound

Procedure

Was prepared according to Method B from 2,4-dichloroquinazoline, N-(4-aminophenyl)-morpholine and 3,5-dimethylpyrazole. Mp. 268.2-270.4° C.

Workup

  1. customWas prepared

Sources & evidence

ORD record
ord-5e3343857ba74e9e891dc14de34d505c
Source dataset
uspto-grants-2012_08
Patent number
US08252806B2

Reaction notes

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