Hydrochloric Acid → HCID 68717438, compound
Reaction equation
[C:1]([O:5][CH2:6][C:7]1[CH:8]=[CH:9][C:10]([N:13]2[C:17](=[O:18])[C:16]([C:19]3[CH:20]=[N:21][CH:22]=[CH:23][CH:24]=3)=[CH:15][NH:14]2)=[N:11][CH:12]=1)([CH3:4])([CH3:3])[CH3:2].[ClH:25]>O1CCOCC1>[ClH:25].[C:1]([O:5][CH2:6][C:7]1[CH:8]=[CH:9][C:10]([N:13]2[C:17](=[O:18])[C:16]([C:19]3[CH:20]=[N:21][CH:22]=[CH:23][CH:24]=3)=[CH:15][NH:14]2)=[N:11][CH:12]=1)([CH3:4])([CH3:2])[CH3:3]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
400 mg (1.2 mmol) of the compound from Example 20 are stirred in 20 ml of a 4 N solution of hydrogen chloride in dioxane at RT for 30 min. The solid is filtered off and dried under high vacuum. It is then dissolved in water, and the solution is lyophilized. The lyophilizate is once more stirred with 10 ml of a 4 N solution of hydrogen chloride in dioxane for 30 min. The solid is filtered off, washed once with tert-butyl methyl ether and dried under high vacuum.
Workup
- filtrationThe solid is filtered off
- customdried under high vacuum
- dissolutionIt is then dissolved in water
- filtrationThe solid is filtered off
- washwashed once with tert-butyl methyl ether
- customdried under high vacuum
Sources & evidence
- ORD record
- ord-b0afb485ea3e45be9157f07f629dc3e5
- Source dataset
- uspto-grants-2013_12
- Patent number
- US08609698B2
Reaction notes
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