참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Pyridine | HCID 1049 | — |
| 반응물 | Methanesulfonyl chloride | HCID 31297 | — |
| 반응물 | (R)-4-bromo-alpha-methylbenzylamine | HCID 853000 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N-[(1R)-1-(4-bromophenyl)ethyl]methanesulfonamide | HCID 28560458 | 58% |
반응 단계
To a stirred solution of (R)-(+)-1-(4-bromophenyl)ethylamine (0.5 g, 2.49 mmol), in anhydrous CH2Cl2 (5 mL) under argon were added methane sulfonyl chloride (0.23 mL, 2.99 mmol) and Pyridine (0.30 mL, 3.73 mmol). The resulting solution was stirred at 25° C. for 3 hrs. The reaction mixture was quenched with 1 N HCl and extracted with EtOAc (30 mL). The organic phase was washed with brine (50 mL), dried over Na2SO4 and evaporated. The residue was purified by flash column chromatography (80% EtOAc in hexanes) to give the product (0.40 g, 58%) as a white solid.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07148226B2 |
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| 출처 데이터셋 | uspto-grants-2006_12 |
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| ORD ID | ord-efb1bf49ff7544b984f4837cf26f0507 |
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| 출처 메모 | uspto-grants-2006_12 |
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