O-Methyltyramine → HCID 131716192, compound

HRID 981584Notes

Reaction equation

HRID 981584 reaction equation
[NH:1]([C:17]([O:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[O:18])[C@H:2]([C:14]([OH:16])=[O:15])[CH2:3][C:4](=[O:13])[O:5][CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.C1CCC(N=C=NC2CCCCC2)CC1.[CH3:39][O:40][C:41]1[CH:46]=[CH:45][C:44]([CH2:47][CH2:48][NH2:49])=[CH:43][CH:42]=1>C(Cl)Cl>[NH:1]([C:17]([O:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[O:18])[C@H:2]([C:14]([OH:16])=[O:15])[CH2:3][C:4](=[O:13])[O:5][CH2:6][C:7]1[CH:12]=[CH:11][CH:10]=[CH:9][CH:8]=1.[CH3:39][O:40][C:41]1[CH:46]=[CH:45][C:44]([CH2:47][CH2:48][NH-:49])=[CH:43][CH:42]=1

Participants

5

Procedure

Boc-Asp(OBzl)-OH (38.8 g; 0.12 Mole) was dissolved in CH2Cl2 (250 ml) and cooled in a dry ice/acetone bath. DCC (24.75 g: 0.12 Mole) dissolved in CH2Cl2 (50 ml) was added slowly. After stirring for 10 minutes 4-methoxyphenylethyl amine(15.1 g; 0.1 Mole) was added dropwise and stirring was continued for another hour at room temperature. The mixture was filtered and the filtrate was washed with saturated NaHCO3 solution (3 x 50 ml) and 1N HCl (50 ml). The organic phase was dried over sodium sulfate and evaporated to an oil. Yield: 41.5 g; FAB-MS: (M+Li)=463.

Workup

  1. temperaturecooled in a dry ice/acetone bath
  2. additionwas added slowly
  3. additionwas added dropwise
  4. waitwas continued for another hour at room temperature
  5. filtrationThe mixture was filtered
  6. washthe filtrate was washed with saturated NaHCO3 solution (3 x 50 ml) and 1N HCl (50 ml)
  7. dry with materialThe organic phase was dried over sodium sulfate
  8. customevaporated to an oil

Sources & evidence

ORD record
ord-cb544e6d826a44e6aa2ca8e26b32328b
Source dataset
uspto-grants-1991_02
Patent number
US04992463

Reaction notes

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