Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 715343생성일: 2026년 10월 25일
Sodium Bicarbonate → (R)-2-methyl-N-(1-(6-(2,2,2-trifluoroethoxy)pyridin-3-yl)ethyl)propane-2-sulfinamide
https://huagongshe.com/reaction/715343
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | Sodium borohydride | HCID 4311764 | — |
| 반응물 | tert-Butylsulfinamide, (R)-(+)- | HCID 10964479 | — |
| 반응물 | Ethanone, 1-[6-(2,2,2-trifluoroethoxy)-3-pyridinyl]- | HCID 58629124 | — |
| 촉매 | Titanium(IV)ethoxide | HCID 2724286 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (R)-2-methyl-N-(1-(6-(2,2,2-trifluoroethoxy)pyridin-3-yl)ethyl)propane-2-sulfinamide | HCID 67510902 | 94% |
반응 단계
A mixture of 1-(6-(2,2,2-trifluoroethoxy)pyridin-3-yl)ethanone (4.51 g, 20.58 mmol, Step-3), (R)-2-methylpropane-2-sulfinamide (3.74 g, 30.9 mmol) and tetraethyl orthotitanate (6.47 mL, 30.9 mmol) in THF (23 mL) is stirred at 70° C. for 17 hours. The reaction mixture is cooled to 0° C., sodium borohydride (2.72 g, 72.0 mmol) is added there, and the mixture is stirred at the same temperature for 1 hour. Saturated aqueous sodium hydrogen carbonate (50 mL) is added to the reaction mixture, and the mixture is stirred for 10 minutes. After filtration through a pad of Celite™, the filtrate is extracted with EtOAc (300 mL). The organic layer is washed with water (100 mL×2) and dried over sodium sulfate. After filtration, the filtrate is concentrated in vacuo. The residue is purified by column chromatography on silica gel eluting with n-hexane/EtOAc (4:1 to 1:1) to give 6.25 g (94% yield) of the title compound as colorless oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09187475B2 |
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| 출처 데이터셋 | uspto-grants-2015_11 |
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| ORD ID | ord-8ac734a53f2547ec944670887b4578ac |
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| 출처 메모 | uspto-grants-2015_11 |
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