참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Thionyl Chloride | HCID 24386 | — |
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | (R)-N-(2-pyridyl)-2-aminopropanol | HCID 21339422 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (R)-4-methyl-3-(2-pyridyl)-[1,2,3]oxathiazolidine 2-oxide | HCID 54573470 | 59.8% |
반응 단계
A solution of (R)-N-(2-pyridyl)-2-aminopropanol (20.0 g, 0.13 moles) and N,N-diisopropylethylamine (33.6 g, 0.13 moles) in dichloromethane (500 ml) was cooled to 5° C. Then thionyl chloride (15.5 g, 0.13 moles) in dichloromethane (100 ml) was added slowly whilst the temperature was kept below 10° C. The mixture was stirred for 0.5 h. and ice cold water (500 ml) was added. The organic phase was separated and washed with water (5×500 ml). The aqueous phase was back-extracted with dichloromethane (2×500 ml), the organic phases were combined, dried (MgSO4) and evaporated in vacuo to give a brown oil. This was purified on a silica column, eluting with diethyl ether to give (R)-4-methyl-3-(2-pyridyl)-[1,2,3]oxathiazolidine 2-oxide (15.4 g) as a clear oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06133449 |
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| 출처 데이터셋 | uspto-grants-2000_10 |
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| ORD ID | ord-daeb6f58e7784fc0bd7f868cac17917d |
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| 출처 메모 | uspto-grants-2000_10 |
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