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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 471850생성일: 2026년 10월 25일

Nitrogen → 1,1-dimethylethyl 6-[3-(aminocarbonyl)phenyl]-3,4-dihydro-2(1H)-isoquinolinecarboxylate

https://huagongshe.com/reaction/471850

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물(3-Carbamoylphenyl)boronic acidHCID 2737814—
반응물Tert-butyl 6-(trifluoromethylsulfonyloxy)-3,4-dihydroisoquinoline-2(1H)-carboxylateHCID 10091216—
촉매HCID 178418397HCID 178418397—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물1,1-dimethylethyl 6-[3-(aminocarbonyl)phenyl]-3,4-dihydro-2(1H)-isoquinolinecarboxylateHCID 58276342—

반응 조건

온도100 °C

반응 단계

A solution of 3-(aminocarbonyl)phenyl boronic acid (0.663 g; 4.0 mmol), 1,1-dimethylethyl 6-{[(trifluoromethyl)sulfonyl]oxy}-3,4-dihydro-2(1H)-isoquinoline carboxylate (1.28 g; 3.35 mmol; Ex V-16) in DMF (10 mL) was sparged with N2 for 10 min, K3PO4 (1.7 g; 8.0 mmol) and Pd(PPh3)4 (0.193 g; 0.17 mmol) were added and the mixture was stirred at 100° C. for 2 h. Upon cooling, the mixture was poured into water and extracted with EtOAc (×3). Combined organics were washed (H2O, brine), and dried over Na2SO4. Residual solids were collected from the aqueous layer by filtration, air-dried, dissolved in hot EtOH and combined with the dried EtOAc extracts. The whole was adsorbed onto a minimal amount of silica gel and purified by flash chromatography (EtOAc/hexanes), affording the title compound as a as a colorless solid. LC/MS (method B) 2.69 min; m/z 297 ([M−C4H8]+H, 70%), 253 ([M−Boc]+H, 74%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08633175B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-a25894fdf5e94c298324b42f90c6b2f1
출처 메모uspto-grants-2014_01