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Ethyl Acetate → (S)-2-{(S)-2-[(S)-3-(4-Allyloxy-phenyl)-2-(4-fluoro-benzenesulfonylamino)-propionylamino]-4-methyl-pentanoylamino}-pent-4-enoic acid methyl ester

HRID 2371308
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Reaktionsgleichung

Reaktionsgleichung von HRID 2371308
[CH2:1]([O:4][C:5]1[CH:10]=[CH:9][C:8]([CH2:11][C@H:12]([NH:24][S:25]([C:28]2[CH:33]=[CH:32][C:31]([F:34])=[CH:30][CH:29]=2)(=[O:27])=[O:26])[C:13]([NH:15][C@@H:16]([CH2:20][CH:21]([CH3:23])[CH3:22])[C:17]([OH:19])=O)=[O:14])=[CH:7][CH:6]=1)[CH:2]=[CH2:3].CN(C(ON1N=N[C:45]2[CH:46]=CC=N[C:44]1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.CC[N:61](C(C)C)C(C)C.C[CH2:69][O:70][C:71]([CH3:73])=[O:72]>CN(C=O)C>[CH3:69][O:70][C:71](=[O:72])[C@@H:73]([NH:61][C:17](=[O:19])[C@@H:16]([NH:15][C:13](=[O:14])[C@@H:12]([NH:24][S:25]([C:28]1[CH:29]=[CH:30][C:31]([F:34])=[CH:32][CH:33]=1)(=[O:27])=[O:26])[CH2:11][C:8]1[CH:9]=[CH:10][C:5]([O:4][CH2:1][CH:2]=[CH2:3])=[CH:6][CH:7]=1)[CH2:20][CH:21]([CH3:23])[CH3:22])[CH2:46][CH:45]=[CH2:44]
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Komponenten

6

Edukt 4

HCID 8857Ethyl AcetateHCID 81531DiisopropylethylamineHCID 9886157Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 66846978HCID 66846978, Verbindung

Produkt 1

HCID 66846969
(S)-2-{(S)-2-[(S)-3-(4-Allyloxy-phenyl)-2-(4-fluoro-benzenesulfonylamino)-propionylamino]-4-methyl-pentanoylamino}-pent-4-enoic acid methyl ester

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

Carboxylic acid 12 (2.50 g, 5.08 mmol), HATU (2.13 g, 5.59 mmol) and (S)-allyl-glycine methyl ester hydrochloride (0.925 g, 5.59 mmol) were dissolved in DMF (30 mL). DIPEA was added (3.54 mL, 20.3 mmol) and the reaction mixture was stirred at rt for 18 h before being partitioned between EtOAc and 1M hydrochloric acid. The organic phase was washed sequentially with 1M hydrochloric acid and brine before being dried (MgSO4), filtered and concentrated in vacuo. Purification was achieved using flash chromatography, eluting with a gradient of (50/70) petroleum ether to 2/1 EtOAc/(50/70) petroleum ether to yield a white solid, 2.70 g, 89%. Rf=0.38 (1/1 EtOAc/(50/70) petroleum ether).

Aufarbeitung

  1. custombefore being partitioned between EtOAc and 1M hydrochloric acid
  2. washThe organic phase was washed sequentially with 1M hydrochloric acid and brine
  3. dry with materialbefore being dried (MgSO4)
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. customPurification
  7. washeluting with a gradient of (50/70) petroleum ether to 2/1 EtOAc/(50/70) petroleum ether
  8. customto yield a white solid, 2.70 g, 89%

Quellen und Nachweise

ORD-Eintrag
ord-04bf3d20d7d1431ba9b726785779c9c8
Quelldatensatz
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08710178B2

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