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HRID 36848Erstellt: 24. Oktober 2026

Oxygen → 2H-Pyrimido[4,5-b][1,4]benzothiazine-2,4(3H)-dione

https://huagongshe.com/de/reaction/36848

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktOxygenHCID 977—
EduktQuinoneHCID 4650—
Edukt2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
EduktDiethyl azodicarboxylateHCID 5462977—
Edukt1,5-dihydro-2H-pyrimido[4,5-b][1,4]benzothiazine-2,4(3H)-dioneHCID 12362526—
EduktHCID 178418361HCID 178418361—
LösungsmittelAcetonitrileHCID 6342—
Produkt2H-Pyrimido[4,5-b][1,4]benzothiazine-2,4(3H)-dioneHCID 13584315—

Reaktionsschritte

When derivative compounds of formula (II) are desired, a solution or suspension of 1,5-dihydro-2H-pyrimido[4,5-b][1,4]benzothiazine-2,4(3H)-dione derivative of formula (I) wherein R4 is hydrogen in acetonitrile is prepared. To that solution or suspension at room temperature is added, dropwise, an oxidant such as diethylazodicarboxylate, 1,4-benzoquinone or 2,3-dichloro-5,6-dicyano-1,4-benzoquinone. Alternatively, oxygen can be used as the oxidant. A preferred oxidant is diethylazodicarboxylate. The reaction mixture is stirred. When a precipitate results, the precipitate is collected an washed with diethylether to give a 2H-pyrimido[4,5-b][1,4]benzothiazine-2,4(3H)-dione derivative of formula (II). When no precipitate is obtained after oxidation, the solvent is removed from the reaction mixture, and the residue is triturated with diethylether and filtered to give a compound of formula (II).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05418231
Quelldatensatzuspto-grants-1995_05
ORD IDord-55b65922f3b64bb19f3ef7abffd4a7bc
Quellennotizuspto-grants-1995_05