Hydrochloric Acid → 2-[5-(2,2-Dimethylpropoxy)pyridin-2-yl]-4-(1H-imidazol-1-yl)-1,2-dihydro-3H-pyrazol-3-one hydrochloride
Reaction equation
[ClH:1].[CH3:2][C:3]([CH3:24])([CH3:23])[CH2:4][O:5][C:6]1[CH:7]=[CH:8][C:9]([N:12]2[C:16](=[O:17])[C:15]([N:18]3[CH:22]=[CH:21][N:20]=[CH:19]3)=[CH:14][NH:13]2)=[N:10][CH:11]=1>O1CCOCC1>[ClH:1].[CH3:2][C:3]([CH3:24])([CH3:23])[CH2:4][O:5][C:6]1[CH:7]=[CH:8][C:9]([N:12]2[C:16](=[O:17])[C:15]([N:18]3[CH:22]=[CH:21][N:20]=[CH:19]3)=[CH:14][NH:13]2)=[N:10][CH:11]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
5 ml of a 4 N solution of hydrogen chloride in dioxane are added to 200 mg (0.638 mmol) of the compound from Example 92 and the mixture is stirred at RT for 30 min. The solid is subsequently filtered off, washed once with dioxane and twice with tert-butyl methyl ether and subsequently dried under a high vacuum.
Workup
- filtrationThe solid is subsequently filtered off
- washwashed once with dioxane and twice with tert-butyl methyl ether
- customsubsequently dried under a high vacuum
Sources & evidence
- ORD record
- ord-8fc1266baa554ad18da2eeff6955f798
- Source dataset
- uspto-grants-2015_10
- Patent number
- US09168249B2
Reaction notes
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