참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Oxygen | HCID 977 | — |
| 반응물 | Quinone | HCID 4650 | — |
| 반응물 | 2,3-Dichloro-5,6-dicyano-1,4-benzoquinone | HCID 6775 | — |
| 반응물 | Diethyl azodicarboxylate | HCID 5462977 | — |
| 반응물 | 1,5-dihydro-2H-pyrimido[4,5-b][1,4]benzothiazine-2,4(3H)-dione | HCID 12362526 | — |
| 반응물 | HCID 178418361 | HCID 178418361 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 2H-Pyrimido[4,5-b][1,4]benzothiazine-2,4(3H)-dione | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05418231 |
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| 출처 데이터셋 | uspto-grants-1995_05 |
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| ORD ID | ord-55b65922f3b64bb19f3ef7abffd4a7bc |
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| 출처 메모 | uspto-grants-1995_05 |
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