3,5-Dimethylpyrazole → HCID 131729931, compound

HRID 889100Notes

Reaction equation

HRID 889100 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.[CH:13]1([OH:19])[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1.[CH3:20][C:21]1[CH:25]=[C:24]([CH3:26])[NH:23][N:22]=1>>[ClH:1].[CH:13]1([O:19][C:10]2[C:9]3[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=3)[N:3]=[C:2]([N:22]3[C:21]([CH3:20])=[CH:25][C:24]([CH3:26])=[N:23]3)[N:11]=2)[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]1

Participants

4

Reactant 3

HCID 62103,5-DimethylpyrazoleHCID 7966CyclohexanolHCID 2528862,4-Dichloroquinazoline

Product 1

HCID 131729931HCID 131729931, compound

Procedure

Was prepared according to Method A from 2,4-dichloroquinazoline, cyclohexanol and 3,5-dimethylpyrazole. Mp. 152.9-153.5° C.

Workup

  1. customWas prepared

Sources & evidence

ORD record
ord-023007fdd5884ada9349baf22dae6be1
Source dataset
uspto-grants-2012_08
Patent number
US08252806B2

Reaction notes

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