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HRID 36848作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物OxygenHCID 977—
反応物QuinoneHCID 4650—
反応物2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
反応物Diethyl azodicarboxylateHCID 5462977—
反応物1,5-dihydro-2H-pyrimido[4,5-b][1,4]benzothiazine-2,4(3H)-dioneHCID 12362526—
反応物HCID 178418361HCID 178418361—
溶媒AcetonitrileHCID 6342—
生成物2H-Pyrimido[4,5-b][1,4]benzothiazine-2,4(3H)-dioneHCID 13584315—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05418231
出典データセットuspto-grants-1995_05
ORD IDord-55b65922f3b64bb19f3ef7abffd4a7bc
出典メモuspto-grants-1995_05