Methylamine hydrochloride → HCID 59831810, compound

HRID 1716642Notes

Reaction equation

HRID 1716642 reaction equation
[CH3:1][NH2:2].Cl.C[Al](C)C.CO[C:10](=[O:30])[CH2:11][CH:12]([C:21]1[CH:29]=[C:28]2[C:24]([CH:25]=[CH:26][NH:27]2)=[CH:23][CH:22]=1)[C:13]1[CH:18]=[CH:17][CH:16]=[C:15]([O:19][CH3:20])[CH:14]=1>C1C=CC=CC=1.Cl>[NH:27]1[C:28]2[C:24](=[CH:23][CH:22]=[C:21]([CH:12]([C:13]3[CH:18]=[CH:17][CH:16]=[C:15]([O:19][CH3:20])[CH:14]=3)[CH2:11][C:10]([NH:2][CH3:1])=[O:30])[CH:29]=2)[CH:25]=[CH:26]1

Participants

6

Conditions

Temperature
5 °C

Procedure

To a 5° C. stirring suspension of MeNH2.HCl (70 mg, 1.04 mmol) in benzene (1 ml) was added Me3Al (2M in toluene, 0.52 ml, 1.04 mmol) dropwise. The reaction mixture was stirred at RT for 1 h and a solution of 3-(1H-indol-6-yl)-3-(3-methoxy-phenyl)-propionic acid methyl ester XXXI (160 mg, 0.52 mmol) in benzene (5 ml) was added. The mixture was stirred at 90° C. for 4 h, cooled to RT, and diluted with HCl (5% in water, 6 ml). The resulting mixture was extracted 3 times with EtOAc. The organic layers were combined, washed with H2O (20 ml) and brine (10 ml), dried over MgSO4, filtered, and concentrated to provide 3-(1H-indol-6-yl)-3-(3-methoxy-phenyl)-N-methyl-propionamide XXXII (160 mg, quantitative yield) as a yellow film.

Workup

  1. stirringThe reaction mixture was stirred at RT for 1 h
  2. stirringThe mixture was stirred at 90° C. for 4 h
  3. temperaturecooled to RT
  4. extractionThe resulting mixture was extracted 3 times with EtOAc
  5. washwashed with H2O (20 ml) and brine (10 ml)
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated

Sources & evidence

ORD record
ord-568ebafe293a42b0b856ee8b27d411ca
Source dataset
uspto-grants-2010_09
Patent number
US07803830B2

Reaction notes

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