Dimethylamine → HCID 59582127, compound

HRID 1173803Notes

Reaction equation

HRID 1173803 reaction equation
[CH3:1][O:2][C:3](=[O:27])[C:4]1[CH:9]=[CH:8][C:7]([O:10][CH2:11][CH2:12][NH:13][C:14]([C:16]2[O:17][C:18]3[CH:26]=[CH:25][CH:24]=[CH:23][C:19]=3[C:20]=2[CH2:21]Br)=[O:15])=[CH:6][CH:5]=1.[CH3:28][NH:29][CH3:30].O1CCCC1>ClC1C=CC=CC=1.ClCCl>[CH3:1][O:2][C:3](=[O:27])[C:4]1[CH:9]=[CH:8][C:7]([O:10][CH2:11][CH2:12][NH:13][C:14]([C:16]2[O:17][C:18]3[CH:26]=[CH:25][CH:24]=[CH:23][C:19]=3[C:20]=2[CH2:21][N:29]([CH3:30])[CH3:28])=[O:15])=[CH:6][CH:5]=1

Participants

6

Reactant 3

HCID 674DimethylamineHCID 8028TetrahydrofuranHCID 666882324-{2-[(3-Bromomethylbenzofuran-2-carbonyl)amino]ethoxy}benzoic acid methyl ester

Product 1

HCID 59582127HCID 59582127, compound

Reagents, catalysts & solvents 2

HCID 6344DichloromethaneSolventHCID 7964ChlorobenzeneSolvent

Procedure

A solution of 4-{2-[(3-bromomethylbenzofuran-2-carbonyl)amino]ethoxy}-benzoic acid methyl ester (0.340 mol) in chlorobenzene (200 ml) and dichloromethane (800 ml) was added dropwise to a 0-5° C. solution of 2M dimethylamine in tetrahydrofuran (510 ml, 1.022 mol) over 30 minutes with the temperature below 20° C. The resulting mixture was stirred for one hour and allowed to warm to ambient temperature. After completion of reaction, the reaction mixture was washed with 5% potassium carbonate and water. Solvent was distilled at atmospheric pressure until the pot temperature reached 100° C. After cooling to ˜50° C., acetonitrile (400 ml) and ethyl Acetate (400 ml) were added to the pot. The reaction mixture was heated to reflux until all solids dissolved. The reaction mixture was allowed to cool to give 4-{2-[(3-dimethylaminomethyl-benzofuran-2-carbonyl)amino]ethoxy}benzoic acid methyl ester (76.6 g) as an off white powder.

Workup

  1. customAfter completion of reaction
  2. washthe reaction mixture was washed with 5% potassium carbonate and water
  3. distillationSolvent was distilled at atmospheric pressure until the pot temperature
  4. customreached 100° C
  5. temperatureAfter cooling to ˜50° C.
  6. additionacetonitrile (400 ml) and ethyl Acetate (400 ml) were added to the pot
  7. temperatureThe reaction mixture was heated
  8. temperatureto reflux until all solids
  9. dissolutiondissolved
  10. temperatureto cool

Sources & evidence

ORD record
ord-01f4167e9aeb488a93f87ba4320e7c84
Source dataset
uspto-grants-2010_11
Patent number
US07834054B2

Reaction notes

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