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Triphenylphosphine → Allyl (1S,5R,6S)-1-methyl-2-(1,1-dioxo-2,5,6,7-tetrahydro-1-thia-2,6-diaza-cyclopenta[cd]phenalen-2-ylmethyl)-6-(1-(R)-allyloxycarbonyloxyethyl)-carbapen-2-em-3-carboxylate

HRID 1068564
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1068564
CCOC(/N=N/C(OCC)=O)=O.O[CH2:14][C:15]1[C@H:16]([CH3:38])[C@@H:17]2[C@@H:27]([C@H:28]([O:30][C:31]([O:33][CH2:34][CH:35]=[CH2:36])=[O:32])[CH3:29])[C:26](=[O:37])[N:18]2[C:19]=1[C:20]([O:22][CH2:23][CH:24]=[CH2:25])=[O:21].[S:39]1(=[O:55])(=[O:54])[C:43]2[CH:44]=[CH:45][C:46]3[CH2:47][NH:48][CH2:49][C:50]4[C:53]=3[C:42]=2[C:41](=[CH:52][CH:51]=4)[NH:40]1.C1(P(C2C=CC=CC=2)C2C=CC=CC=2)C=CC=CC=1>O1CCCC1>[CH3:38][C@@H:16]1[C@@H:17]2[C@@H:27]([C@H:28]([O:30][C:31]([O:33][CH2:34][CH:35]=[CH2:36])=[O:32])[CH3:29])[C:26](=[O:37])[N:18]2[C:19]([C:20]([O:22][CH2:23][CH:24]=[CH2:25])=[O:21])=[C:15]1[CH2:14][N:40]1[C:41]2[C:42]3[C:53]4[C:50](=[CH:51][CH:52]=2)[CH2:49][NH:48][CH2:47][C:46]=4[CH:45]=[CH:44][C:43]=3[S:39]1(=[O:55])=[O:54]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 11776TriphenylphosphineHCID 5462977Diethyl azodicarboxylateHCID 11046746allyl (1S,5R,6S)-2-(hydroxymethyl)-6-[1(R)-allyloxycarbonyloxy-ethyl]-1-methylcarbapen-2-em-3-carboxylateHCID 206661122,5,6,7-Tetrahydro-1-thia-2,6-diaza-cyclopenta[cd]phenalene 1,1-dioxide

Produkt 1

HCID 131722705
Allyl (1S,5R,6S)-1-methyl-2-(1,1-dioxo-2,5,6,7-tetrahydro-1-thia-2,6-diaza-cyclopenta[cd]phenalen-2-ylmethyl)-6-(1-(R)-allyloxycarbonyloxyethyl)-carbapen-2-em-3-carboxylate

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

Diethylazodicarboxylate (2.25 mmol) is added to a cold (0° C.) solution of allyl (1S,5R,6S)-2-(hydroxymethyl)-6-[1(R)-allyloxycarbonyloxy-ethyl]-1-methylcarbapen-2-em-3-carboxylate (1.5 mmol), 2,5,6,7-tetrahydro-1-thia-2,6-diaza-cyclopenta[cd]phenalene-1,1-dioxide (1.5 mmol) and triphenylphosphine (2.25 mmol) in tetrahydrofuran (15 mL). The mixture is stirred at room temperature for 30 minutes then partitioned between ethyl acetate (100 mL) and water (100 mL). The water layer is extracted with ethyl acetate (50 mL) and the combined ethyl acetate layers are washed with saturated aqueous sodium chloride (50 mL), dried with magnesium sulfate, filtered, and evaporated. The crude product is purified by column chromatography to give the title compound.

Aufarbeitung

  1. customthen partitioned between ethyl acetate (100 mL) and water (100 mL)
  2. extractionThe water layer is extracted with ethyl acetate (50 mL)
  3. washthe combined ethyl acetate layers are washed with saturated aqueous sodium chloride (50 mL)
  4. dry with materialdried with magnesium sulfate
  5. filtrationfiltered
  6. customevaporated
  7. customThe crude product is purified by column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-672c6f05ad994ee8ad243315865d3d4d
Quelldatensatz
uspto-grants-2001_06
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06251890B1

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