Hydrochloric Acid → HCID 66636711, compound
Reaction equation
[O:1]=[C:2]1[CH2:11][C:10]2=[CH:12][N:13]([CH2:14][C:15]([O:17]CC)=[O:16])[C:8]3[C:9]2=[C:4]([CH:5]=[CH:6][CH:7]=3)[NH:3]1.[OH-].[Li+:21].Cl>C(O)C.O>[O:1]=[C:2]1[CH2:11][C:10]2=[CH:12][N:13]([CH2:14][C:15]([O-:17])=[O:16])[C:8]3[C:9]2=[C:4]([CH:5]=[CH:6][CH:7]=3)[NH:3]1.[Li+:21]Participants
6
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of ethyl (4-oxo-4,5-dihydropyrrolo[4,3,2-de]quinolin-1(3H)-yl)acetate from Step G (79 mg, 0.306 mmol) in ethanol (3 mL) and water (0.5 mL) was added dropwise 1.0 N aqueous lithium hydroxide (0.34 mL, 0.34 mmol). After 5 min, 1 N aqueous HCl was added to adjust the mixture to pH 7 and the solution was concentrated in vacuo to give the title compound. MS: m/z=231 (M+1).
Workup
- concentrationthe solution was concentrated in vacuo
Sources & evidence
- ORD record
- ord-bfe9301e5ce1488da25f4c13a4486a7a
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07696192B2
Reaction notes
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