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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1480129생성일: 2026년 10월 25일

(2S)-1,1,1-Trifluoropropan-2-ol → 5-Cyclopropyl-4-((S)-2,2,2-trifluoro-1-methyl-ethoxy)-pyridine-2-carboxylic acid

https://huagongshe.com/reaction/1480129

반응식

참여 물질

역할이름HCID투입량
반응물(2S)-1,1,1-Trifluoropropan-2-olHCID 6999971—
반응물Potassium tert-butoxideHCID 23665647—
반응물4-Chloro-5-cyclopropylpicolinic acidHCID 90203520—
용매DimethylformamideHCID 6228—
생성물5-Cyclopropyl-4-((S)-2,2,2-trifluoro-1-methyl-ethoxy)-pyridine-2-carboxylic acidHCID 9020457341.7%

반응 단계

To a solution of 4-Chloro-5-cyclopropyl-pyridine-2-carboxylic acid (Example 48b, 0.87 g, 4.4 mmol) in dry DMF (12.0 ml) under an argon atmosphere were added (S)-1,1,1-trifluoropropan-2-ol (CAN 3539-97-7, 1.00 g, 8.8 mmol) and potassium tert-butoxide (1.48 g, 13.2 mmol). The reaction mixture was stirred at room temperature for 30 minutes and stirred at 120° C. for one hour under microwave radiation. DMF was removed in vacuo and the residue was dissolved in ethyl acetate. The solution was extracted with 20 mL of an 2.0M aqueous solution of hydrochloric acid. The organic phase was collected and the aqueous phase was back-extracted with ethyl acetate. The organic phases were combined, dried over sodium sulfate and evaporated down to dryness. The crude material was purified by flash chromatography on silica eluting with a dichloromethane/(3% solution formic acid in methanol) gradient to yield the title compound (505 mg, 33%) as a light brown solid. MS (ESI, m/z): 276.4 (M+H+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09409866B2
출처 데이터셋uspto-grants-2016_08
ORD IDord-2bb9bb390297450bb15dcdca5aaf023e
출처 메모uspto-grants-2016_08