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Dimethylamine → HCID 59582127, compound

HRID 914274
Notes
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Reaction equation

HRID 914274 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
ParticipantsProcedureWorkupSources & evidenceReaction notes

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 6344DichloromethaneSolvent
HCID 7964
Chlorobenzene
Solvent

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-1e67eef3430340f1bf9e210cea430037
Source dataset
uspto-grants-2011_09
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08026371B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes