Hydrochloric Acid → HCID 66596832, compound

HRID 1811390Notes

Reaction equation

HRID 1811390 reaction equation
[H-].[Na+].[CH3:3][O:4][C:5]1[CH:6]=[CH:7][C:8]([CH2:17][CH2:18][CH2:19][CH:20]([C:26]([O:28][CH2:29][CH3:30])=[O:27])[C:21]([O:23][CH2:24][CH3:25])=[O:22])=[C:9]2[C:14]=1[N:13]([CH3:15])[C:12](=[O:16])[CH:11]=[CH:10]2.[H][H].[Cl:33]N1C(=O)CCC1=O.Cl>ClCCl.C1COCC1>[Cl:33][C:20]([CH2:19][CH2:18][CH2:17][C:8]1[CH:7]=[CH:6][C:5]([O:4][CH3:3])=[C:14]2[C:9]=1[CH:10]=[CH:11][C:12](=[O:16])[N:13]2[CH3:15])([C:21]([O:23][CH2:24][CH3:25])=[O:22])[C:26]([O:28][CH2:29][CH3:30])=[O:27]

Participants

8

Reactant 5

HCID 313Hydrochloric AcidHCID 24758Sodium hydrideHCID 31398ChlorosuccinimideHCID 66596895HCID 66596895, compoundHCID 178418361HCID 178418361, compound

Product 1

HCID 66596832HCID 66596832, compoundYield 125.6%

Reagents, catalysts & solvents 2

HCID 6344DichloromethaneSolventHCID 8028TetrahydrofuranSolvent

Procedure

Sodium hydride (60% in oil) (0.33 g) was added under ice cooling to a THF solution (30 ml) of diethyl 2-[3-(8-methoxy-1-methyl-2-oxo-1,2-dihydroquinolin-5-yl)propyl]malonate (2.94 g), and stirring was carried out until the generation of hydrogen stopped. N-chlorosuccinimide (1.2 g) was added, followed by stirring for 2 hours. The reaction mixture was added to cold hydrochloric acid, and extraction with dichloromethane was performed. The extract was dried over anhydrous sodium sulfate, and concentrated under reduced pressure to thereby obtain 4.02 g (yield: quantitative) of diethyl 2-chloro-2-[3-(8-methoxy-1-methyl-2-oxo-1,2-dihydroquinolin-5-yl)propyl]malonate as a yellow oil.

Workup

  1. stirringby stirring for 2 hours
  2. dry with materialThe extract was dried over anhydrous sodium sulfate
  3. concentrationconcentrated under reduced pressure

Sources & evidence

ORD record
ord-b40f401c58bf4cd7ade630d8b25e4268
Source dataset
uspto-grants-2013_01
Patent number
US08362252B2

Reaction notes

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