Hydrochloric Acid → HCID 178517458, compound
Reaction equation
[CH:1]1([C:7]([NH:9][C:10]2[CH:18]=[CH:17][CH:16]=[CH:15][C:11]=2[C:12]([NH2:14])=[O:13])=O)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[OH-].[Na+].Cl>CCO>[CH:1]1([C:7]2[N:14]=[C:12]([OH:13])[C:11]3[C:10](=[CH:18][CH:17]=[CH:16][CH:15]=3)[N:9]=2)[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
2-(Cyclohexylcarbonylamino)benzamide was stirred for 16 h in a mixture of excess 1 M NaOH and EtOH, and the resulting solution was treated with HCl to pH=7 causing the formation of a precipitate. The precipitate was collected by filtration, washed (with water and hexane), and dried under vacuum to give a nearly quantitative yield of 2-cyclohexyl-4-hydroxyquinazoline as a white solid, which was used immediately in the next step.
Workup
- filtrationThe precipitate was collected by filtration
- washwashed (with water and hexane)
- customdried under vacuum
Sources & evidence
- ORD record
- ord-933efebdf0bf4ef5b91b56ef4409fc92
- Source dataset
- uspto-grants-2008_11
- Patent number
- US07452912B2
Reaction notes
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