Hydrogen chloride-ethyl acetate → HCID 67538517, compound

HRID 39929Notes

Reaction equation

HRID 39929 reaction equation
[O:1]1[C:6]2[CH:7]=[CH:8][C:9]([CH2:11][NH:12][CH:13]3[CH2:18][CH2:17][N:16]([CH2:19][CH2:20][N:21]4[C:30]5[C:25](=[C:26]([O:31][CH2:32][C:33]([NH:35][CH3:36])=[O:34])[CH:27]=[CH:28][CH:29]=5)[CH:24]=[CH:23][C:22]4=[O:37])[CH2:15][CH2:14]3)=[CH:10][C:5]=2[O:4][CH2:3][CH2:2]1.[ClH:38].C(OCC)(=O)C>C(OCC)(=O)C>[ClH:38].[O:1]1[C:6]2[CH:7]=[CH:8][C:9]([CH2:11][NH:12][CH:13]3[CH2:14][CH2:15][N:16]([CH2:19][CH2:20][N:21]4[C:30]5[C:25](=[C:26]([O:31][CH2:32][C:33]([NH:35][CH3:36])=[O:34])[CH:27]=[CH:28][CH:29]=5)[CH:24]=[CH:23][C:22]4=[O:37])[CH2:17][CH2:18]3)=[CH:10][C:5]=2[O:4][CH2:3][CH2:2]1

Participants

4

Reactant 2

HCID 21866389Hydrogen chloride-ethyl acetateHCID 59398085HCID 59398085, compound

Product 1

HCID 67538517HCID 67538517, compound

Reagents, catalysts & solvents 1

HCID 8857Ethyl AcetateSolvent

Procedure

To 10 mL of an ethyl acetate solution containing 46 mg of (1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-2-oxo-1,2-dihydroquinolin-5-yloxy)-N-methylacetamide, 0.2 mL of 4 mol/L hydrogen chloride/ethyl acetate was added, and stirred at room temperature for 10 min. The resulting solid was filtered to give 40 mg of (1-(2-(4-((2,3-dihydro-1,4-benzodioxin-6-ylmethyl)amino)piperidin-1-yl)ethyl)-2-oxo-1,2-dihydroquinolin-5-yloxy)-N-methylacetamide hydrochloride as a pale brown solid.

Workup

  1. additionwas added
  2. filtrationThe resulting solid was filtered

Sources & evidence

ORD record
ord-48621128af8542c7aa8154748683da0d
Source dataset
uspto-grants-2013_09
Patent number
US08524738B2

Reaction notes

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