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4-Methylmorpholine → N-[1-(2-t-Butyloxycarbonyl-3-dibenzylaminopropyl)-1-cyclopentane-carbonyl]-O-t-butyl-(S)-tyrosine-t-butyl ester

HRID 1110460
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1110460
[C:1]([O:5][C:6]([CH:8]([CH2:18][N:19]([CH2:27][C:28]1[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=1)[CH2:20][C:21]1[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=1)[CH2:9][C:10]1([C:15]([OH:17])=O)[CH2:14][CH2:13][CH2:12][CH2:11]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].ON1C2C=C[CH:42]=[CH:43][C:38]=2N=N1.[CH2:44](N=C=NCCCN(C)C)C.[C:55]([O:59][C:60](=[O:75])[C@H:61]([CH2:63][C:64]1[CH:69]=[CH:68][C:67]([OH:70])=[CH:66][C:65]=1C(C)(C)C)[NH2:62])([CH3:58])([CH3:57])[CH3:56].CN1CCOCC1>ClCCl>[C:55]([O:59][C:60](=[O:75])[C@H:61]([CH2:63][C:64]1[CH:65]=[CH:66][C:67]([O:70][C:43]([CH3:42])([CH3:38])[CH3:44])=[CH:68][CH:69]=1)[NH:62][C:15]([C:10]1([CH2:9][CH:8]([C:6]([O:5][C:1]([CH3:4])([CH3:2])[CH3:3])=[O:7])[CH2:18][N:19]([CH2:27][C:28]2[CH:29]=[CH:30][CH:31]=[CH:32][CH:33]=2)[CH2:20][C:21]2[CH:26]=[CH:25][CH:24]=[CH:23][CH:22]=2)[CH2:14][CH2:13][CH2:12][CH2:11]1)=[O:17])([CH3:56])([CH3:57])[CH3:58]
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

7

Edukt 5

HCID 79724-MethylmorpholineHCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 757711-HydroxybenzotriazoleHCID 221554593-(1-Carboxycyclopentyl)-2(dibenzylaminomethyl)propanoic acid t-butyl esterHCID 573028330-t-Butyltyrosine t-butyl ester

Produkt 1

HCID 54036042
N-[1-(2-t-Butyloxycarbonyl-3-dibenzylaminopropyl)-1-cyclopentane-carbonyl]-O-t-butyl-(S)-tyrosine-t-butyl ester
Ausbeute 5.768,4 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6344DichloromethaneLösungsmittel

Reaktionsbedingungen

Temperatur
0 °C

Versuchsvorschrift

To an ice cold solution of 1-(2-t-butyloxycarbonyl-3-dibenzylaminopropyl)-1-cyclopentane carboxylic acid (12.7 g, 27 mmole) in dry dichloromethane (100 ml) was added 1-hydroxybenztriazole (4.2 g,.31 mmole), and 1-ethyl-3-(dimethylaminopropyl)-carbodiimide (7 g, 36 mmole) and the resulting solution stirred at 0° C. for 30 minutes. To this solution was added 0-t-butyltyrosine t-butyl ester (8.4 g, 28.6 mmole) and N-methylmorpholine (5.25 g, 52 mmole) and the solution allowed to stand overnight at room temperature. The solvent was evaporated under reduced pressure and the resultant mobile oil was dissolved in methylene chloride and washed with water (2 x ), 2M hydrochloric acid and saturated aqueous sodium bicarbonate (1 x) dried (MgSO4), and the solution filtered and evaporated to yield the crude product as a gum. Recrystallization from n-hexane gave the title compound as a solid (13 g, 69%), m.p. 82-87° C. A further batch of material was obtained by evaporation of the supernatant liquors and further recrystallisation. Found: C,74.12; H,8.69; N,3.87. C45H62N2O6 requires C,74.34; H,8.59; N,3.85%.

Aufarbeitung

  1. waitto stand overnight at room temperature
  2. customThe solvent was evaporated under reduced pressure
  3. dissolutionthe resultant mobile oil was dissolved in methylene chloride
  4. washwashed with water (2 x ), 2M hydrochloric acid and saturated aqueous sodium bicarbonate (1 x)
  5. dry with materialdried (MgSO4)
  6. filtrationthe solution filtered
  7. customevaporated
  8. customto yield the crude product as a gum
  9. customRecrystallization from n-hexane

Quellen und Nachweise

ORD-Eintrag
ord-fdce5d5343454896af4d0210372ca2a1
Quelldatensatz
uspto-grants-1990_12
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US04975444

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