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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 36848생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물OxygenHCID 977—
반응물QuinoneHCID 4650—
반응물2,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 6775—
반응물Diethyl azodicarboxylateHCID 5462977—
반응물1,5-dihydro-2H-pyrimido[4,5-b][1,4]benzothiazine-2,4(3H)-dioneHCID 12362526—
반응물HCID 178418361HCID 178418361—
용매AcetonitrileHCID 6342—
생성물2H-Pyrimido[4,5-b][1,4]benzothiazine-2,4(3H)-dioneHCID 13584315—

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05418231
출처 데이터셋uspto-grants-1995_05
ORD IDord-55b65922f3b64bb19f3ef7abffd4a7bc
출처 메모uspto-grants-1995_05