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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1914595생성일: 2026년 10월 27일

Diisopropylethylamine → (4,4-Difluoro-azepan-1-yl)-(5-oxazol-4-yl-thiophen-3-yl)-methanone

https://huagongshe.com/reaction/1914595

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물5-Oxazol-4-yl-thiophene-3-carboxylic acidHCID 58110221—
반응물4,4-Difluoro-azepane trifluoroacetateHCID 66849847—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물(4,4-Difluoro-azepan-1-yl)-(5-oxazol-4-yl-thiophen-3-yl)-methanoneHCID 4422648130.9%

반응 단계

4,4-Difluoro-azepane trifluoroacetate (Synthesis 47, 0.113 g, 0.45 mmol) was dissolved in THF (1 mL) and added to 5-oxazol-4-yl-thiophene-3-carboxylic acid (0.059 g, 0.30 mmol). DIPEA (0.154 mL, 0.90 mmol) was added followed by HATU (0.125 g, 0.33 mmol) and the reaction mixture was then stirred at room temperature overnight. The mixture was diluted with DCM then washed with aqueous sodium carbonate solution. The organics were dried over sodium sulfate, filtered and evaporated. The crude material was purified by HPLC, eluting with 5%-98% methanol in water (0.1% formic acid). The fractions containing the desired product were freeze-dried to give the title compound (0.029 g). LCMS m/z 313.15 [m+H]+ R.T.=8.31 min (Analytical Method 10).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08614209B2
출처 데이터셋uspto-grants-2013_12
ORD IDord-8a72e6a1b1d3470584d88c1e573aeb08
출처 메모uspto-grants-2013_12