반응 #2467953

ord-33066712eb4d4db8a40659289cebd0b7

반응 방정식

CC(=O)NC(C)C(=O)N[C@@H](Cc1ccccc1)C(=O)O
N-[2-(Acetylamino)propionyl]phenylalanine
CCN=C=NCCCN(C)C.Cl
1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride
On1nnc2ccccc21
1-hydroxybenzotriazole
C1CCNCC1
piperidine
CC(=O)NC(C)C(=O)NC(Cc1ccccc1)C(=O)N1CCCCC1
1-{2-[N-(2-(acetylamino)propionyl)amino]-3-phenylpropionyl}piperidine

반응 조건

온도
50°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타Fog 24 hours
  2. 2
    추출the resulting mixture is extracted three times with chloroform
  3. 3
    세척The organic layer is washed with 10% hydrochloric acid
  4. 4
    건조a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate
  5. 5
    workup.DISTILLATIONAfter the solvent is distilled away under reduced pressure
  6. 6
    기타the residue is purified by silica gel column chromatography

실험 절차

N-[2-(Acetylamino)propionyl]phenylalanine obtained in Experimental Example 21 (10 mg, 0.036 mmol) is suspended in N,N-dimethylformamide (5 ml), and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (14 mg, 0.073 mmol), 1-hydroxybenzotriazole (15 mg, 0.11 mmol) and piperidine (40 μl, 0.40 mmol) are added to the suspension at room temperature, followed by stirring at 50° C. Fog 24 hours. To the reaction mixture is added water, and the resulting mixture is extracted three times with chloroform. The organic layer is washed with 10% hydrochloric acid and a saturated aqueous solution of sodium chloride, and dried over anhydrous magnesium sulfate. After the solvent is distilled away under reduced pressure, the residue is purified by silica gel column chromatography to obtain 1-{2-[N-(2-(acetylamino)propionyl)amino]-3-phenylpropionyl}piperidine.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US08257943B2uspto-grants-2012_09