Formic Acid → Ethyl 2-(2-aminothiazol-4-yl)-2-propargyloxyiminoacetate

HRID 364496Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 364496
C(O)=O.C([NH:23][C:24]1[S:25][CH:26]=[C:27]([C:29](=[N:35][O:36][CH2:37][C:38]#[CH:39])[C:30]([O:32][CH2:33][CH3:34])=[O:31])[N:28]=1)(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>O1CCCC1>[NH2:23][C:24]1[S:25][CH:26]=[C:27]([C:29](=[N:35][O:36][CH2:37][C:38]#[CH:39])[C:30]([O:32][CH2:33][CH3:34])=[O:31])[N:28]=1

Komponenten

4

Edukt 2

HCID 284Formic AcidHCID 54124335Ethyl 2-(2-tritylaminothiazol-4-yl)-2-propargyloxyiminoacetate

Produkt 1

HCID 53907014Ethyl 2-(2-aminothiazol-4-yl)-2-propargyloxyiminoacetateAusbeute 7,2 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Reaktionsbedingungen

Temperatur
60 °C

Versuchsvorschrift

50% Formic acid (41 ml.) was added to a solution of ethyl 2-(2-tritylaminothiazol-4-yl)-2-propargyloxyiminoacetate (syn isomer, 8.2 g.) and tetrahydrofuran (41 ml.), and stirred at 60° C. for an hour. The resultant solution was concentrated to a half of initial volume under reduced pressure, and the precipitates were collected by filtration and washed with diisopropyl ether. The filtrate and washing solution were combined together and concentrated in vacuo. The residue was added to ethyl acetate (200 ml.) under stirring. The insoluble substance was collected by filtration, and washed with diethyl ether to give ethyl 2-(2-aminothiazol-4-yl)-2-propargyloxyiminoacetate (syn isomer, 0.3 g.). The filtrate and ethyl acetate washing solution were combined together, washed with a saturated aqueous solution of sodium bicarbonate and a saturated aqueous solution of sodium chloride twice in turn, and dried over magnesium sulfate. The solution was treated with activated charcoal and concentrated in vacuo. The residue was dried in vacuo after adding benzene. The residue was subjected to column chromatography on silica gel with benzene and ethyl acetate in turn. The eluate was concentrated in vacuo, and the residue was triturated with diisopropyl ether. The precipitates were collected by filtration, washed with diisopropyl ether to give the same compound as mentioned above (syn isomer, 2.658 g.). The I.R. spectrum and N.M.R. spectrum are the same as those of the compound obtained in Example I-(3).

Aufarbeitung

  1. concentrationThe resultant solution was concentrated to a half of initial volume under reduced pressure
  2. filtrationthe precipitates were collected by filtration
  3. washwashed with diisopropyl ether
  4. washThe filtrate and washing solution
  5. concentrationconcentrated in vacuo
  6. additionThe residue was added to ethyl acetate (200 ml.)
  7. stirringunder stirring
  8. filtrationThe insoluble substance was collected by filtration
  9. washwashed with diethyl ether

Quellen und Nachweise

ORD-Eintrag
ord-a4234ee98060418c8279e2b80508b387
Quelldatensatz
uspto-grants-1986_08
Patentnummer
US04604456

Notizen zur Reaktion

Wird geladen…