Hydrogen chloride-ethyl acetate → HCID 66892797, compound

HRID 1513578Notes

Reaction equation

HRID 1513578 reaction equation
[CH3:1][N:2]([CH3:34])[CH2:3][CH2:4][N:5]([CH3:33])[C:6]([C:8]1[S:20][C:19]2[C:18]3[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=3[N:12]([CH2:21][C:22](=[O:29])[C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)[C:11](=[O:30])[C:10]=2[C:9]=1[O:31][CH3:32])=[O:7].C(OC(=O)C)C.[ClH:41]>C(OCC)(=O)C>[ClH:41].[CH3:1][N:2]([CH3:34])[CH2:3][CH2:4][N:5]([CH3:33])[C:6]([C:8]1[S:20][C:19]2[C:18]3[CH:17]=[CH:16][CH:15]=[CH:14][C:13]=3[N:12]([CH2:21][C:22](=[O:29])[C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)[C:11](=[O:30])[C:10]=2[C:9]=1[O:31][CH3:32])=[O:7]

Participants

4

Procedure

To a solution of the N-[2-(dimethylamino)ethyl]-3-methoxy-N-methyl-4-oxo-5-(2-oxo-2-phenylethyl)-4,5-dihydrothieno[3,2-c]quinoline-2-carboxamide (180 mg, 0.38 mmol) in ethyl acetate (10 mL) was added 4N hydrogen chloride ethyl acetate solution (0.1 mL), and the obtained precipitate was collected by filtration, washed with diethyl ether, and dried under reduced pressure to give the title compound (144 mg, 55%) as a white powder.

Workup

  1. filtrationthe obtained precipitate was collected by filtration
  2. washwashed with diethyl ether
  3. customdried under reduced pressure

Sources & evidence

ORD record
ord-ea2325ebedb645ef89faf670a31c3261
Source dataset
uspto-grants-2012_07
Patent number
US08217176B2

Reaction notes

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