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Diethyl (ethoxymethylene)malonate → Ethyl 1,6-dihydro-1-(2-methoxyethyl)-6-oxo-2-(3-thienyl)-5-pyrimidinecarboxylate

HRID 714427
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 714427
[CH3:1][O:2][CH2:3][CH2:4][NH2:5].Cl.C(O[C:10]([C:12]1[CH:16]=[CH:15][S:14][CH:13]=1)=[NH:11])C.[O-]CC.[Na+].C([O:23][CH:24]=[C:25]([C:31](OCC)=O)[C:26]([O:28][CH2:29][CH3:30])=[O:27])C>CO>[CH3:1][O:2][CH2:3][CH2:4][N:5]1[C:24](=[O:23])[C:25]([C:26]([O:28][CH2:29][CH3:30])=[O:27])=[CH:31][N:11]=[C:10]1[C:12]1[CH:16]=[CH:15][S:14][CH:13]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

6

Edukt 4

HCID 6871Diethyl (ethoxymethylene)malonateHCID 80182-MethoxyethylamineHCID 2723922Sodium ethoxideHCID 122310463-Thiophenecarboximidic acid ethyl ester hydrochloride

Produkt 1

HCID 67954683Ethyl 1,6-dihydro-1-(2-methoxyethyl)-6-oxo-2-(3-thienyl)-5-pyrimidinecarboxylateAusbeute 59 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 887MethanolLösungsmittel

Versuchsvorschrift

2-Methoxy-1-ethylamine (0.86 g, 11.4 mmol) was added to a solution of 3-thiophenecarboximidic acid ethyl ester hydrochloride (2.0 g, 10.4 mmol) in methanol (10 mL), which was then stirred at ambient temperature for 1.5 h. The reaction mixture was then concentrated under reduced pressure and redissolved in ethanol (10 mL). Sodium ethoxide solution (21% w/w in ethanol, 3.4 g, 10 mmol) and diethyl ethoxymethylenemalonate (2.2 g, 10 mmol) were added and the mixture was heated to reflux for 2 h before being concentrated under reduced pressure and purified by medium pressure liquid chromatography on silica gel eluting with 0 to 100% ethyl acetate in hexanes to provide 1.82 g of the title compound as an oil.

Aufarbeitung

  1. concentrationThe reaction mixture was then concentrated under reduced pressure
  2. dissolutionredissolved in ethanol (10 mL)
  3. temperaturethe mixture was heated
  4. temperatureto reflux for 2 h
  5. concentrationbefore being concentrated under reduced pressure
  6. custompurified by medium pressure liquid chromatography on silica gel eluting with 0 to 100% ethyl acetate in hexanes

Quellen und Nachweise

ORD-Eintrag
ord-7834bbf3631448ec96a6258f1b6ce942
Quelldatensatz
uspto-grants-2015_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US09187432B2

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