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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 36848Generated: October 27, 2026

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

https://huagongshe.com/reaction/36848

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxygenHCID 977—
ReactantQuinoneHCID 4650—
Reactant2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
ReactantDiethyl azodicarboxylateHCID 5462977—
Reactant1,5-dihydro-2H-pyrimido[4,5-b][1,4]benzothiazine-2,4(3H)-dioneHCID 12362526—
ReactantHCID 178418361HCID 178418361—
SolventAcetonitrileHCID 6342—
Product2H-Pyrimido[4,5-b][1,4]benzothiazine-2,4(3H)-dioneHCID 13584315—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05418231
Source datasetuspto-grants-1995_05
ORD IDord-55b65922f3b64bb19f3ef7abffd4a7bc
Source noteuspto-grants-1995_05