Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1439861생성일: 2026년 10월 27일
Ethyl Acetate → (R)-2-(4-Chlorophenyl)-4-[(S)-N-(2-naphthalene-sulfonyl)prolyl]-3,4-dihydro-2H-1,4-benzothiazine
https://huagongshe.com/reaction/1439861
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ethyl Acetate | HCID 8857 | — |
| 반응물 | 2-(4-chlorophenyl)-3,4-dihydro2H-1,4-benzothiazine | HCID 13071524 | — |
| 반응물 | (S)-N-(2-naphthalenesulfonyl)prolyl chloride | HCID 13576782 | — |
| 용매 | Pyridine | HCID 1049 | — |
| 생성물 | (R)-2-(4-Chlorophenyl)-4-[(S)-N-(2-naphthalene-sulfonyl)prolyl]-3,4-dihydro-2H-1,4-benzothiazine | HCID 54249707 | 51.5% |
반응 단계
To a solution of (±)-2-(4-chlorophenyl)-3,4-dihydro-2H-1,4-benzothiazine (10.01 g, 0.038 mole) in pyridine (150 ml) is added (S)-N-(2-naphthalenesulfonyl)prolyl chloride (18.57 g, 0.057 mole), and the mixture is stirred at room temperature for 4 hours. To the reaction mixture is added ethyl acetate, and the mixture is washed with 5% hydrochloric acid, water, aqueous sodium hydrogen carbonate solution, water and saline in this order, and the ethyl acetate layer is separated, dried over sodium sulfate and distilled to remove the solvent. The resulting caramel is subjected to silica gel column chromatography (hexane: ethyl acetate=5:1-3:1). From the fraction eluted first there is obtained (R)-2-(4-chlorophenyl)-4-[(S)-N-(2-naphthalenesulfonyl)prolyl]-3,4-dihydro-2H-1,4-benzothiazine (10.75 g, 51%) as crystals. M.p. 147°-151° C.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05496815 |
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| 출처 데이터셋 | uspto-grants-1996_03 |
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| ORD ID | ord-2cce93ec24f04d879d69f95f85e98f8f |
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| 출처 메모 | uspto-grants-1996_03 |
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