Morpholine → HCID 69199563, compound

HRID 1745806Notes

Reaction equation

HRID 1745806 reaction equation
[NH:1]1[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.[CH2:7]([O:9][C:10](=[O:27])[CH2:11][C:12]1[C:21]2[C:16](=[CH:17][C:18]([O:24][CH3:25])=[C:19]([O:22][CH3:23])[CH:20]=2)[C:15](Cl)=[N:14][CH:13]=1)[CH3:8]>C1(C)C=CC=CC=1>[CH2:7]([O:9][C:10](=[O:27])[CH2:11][C:12]1[C:21]2[C:16](=[CH:17][C:18]([O:24][CH3:25])=[C:19]([O:22][CH3:23])[CH:20]=2)[C:15]([N:1]2[CH2:6][CH2:5][O:4][CH2:3][CH2:2]2)=[N:14][CH:13]=1)[CH3:8]

Participants

4

Reactant 2

HCID 8083MorpholineHCID 86588461HCID 86588461, compound

Product 1

HCID 69199563HCID 69199563, compound

Reagents, catalysts & solvents 1

HCID 1140TolueneSolvent

Procedure

Excess morpholine is added to a suspension of (1-chloro-6,7-dimethoxy-isoquinolin-4-yl)-acetic acid ethyl ester (0.200 g, 0.65 mmol) in toluene (1 ml) and the mixture heated to reflux until the starting material is consumed. After evaporation, the residue is partitioned between water and dichloromethane, the organic phase is dried over magnesium sulfate and evaporated. to afford (6,7-dimethoxy-1-morpholin-4-yl-isoquinolin-4-yl)-acetic acid ethyl ester [MH]+ 361. The crude ester (0.240 g, 0.66 mmol) is dissolved in ethanol (20 ml), treated with 2M sodium hydroxide (3 ml) and stirred at room temperature overnight. After adjustment to pH 1 with concentrated hydrochloric acid, the solvent is evaporated and the crude acid used directly for formation of the xanthine derivative.

Workup

  1. temperaturethe mixture heated
  2. temperatureto reflux until the starting material
  3. customis consumed
  4. customAfter evaporation
  5. customthe residue is partitioned between water and dichloromethane
  6. dry with materialthe organic phase is dried over magnesium sulfate
  7. customevaporated

Sources & evidence

ORD record
ord-67362af270c74eed8f1ca95dcd991754
Source dataset
uspto-grants-2006_03
Patent number
US07019136B2

Reaction notes

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