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HRID 70315作成日:2026年10月26日

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

https://huagongshe.com/reaction/70315

反応式

関与物質

役割名称HCID仕込み量
反応物NitrogenHCID 947—
反応物Potassium Phosphate, TribasicHCID 62657—
反応物(3-Carbamoylphenyl)boronic acidHCID 2737814—
反応物Tert-butyl 6-(trifluoromethylsulfonyloxy)-3,4-dihydroisoquinoline-2(1H)-carboxylateHCID 10091216—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
溶媒DimethylformamideHCID 6228—
生成物1,1-dimethylethyl 6-[3-(aminocarbonyl)phenyl]-3,4-dihydro-2(1H)-isoquinolinecarboxylateHCID 58276342—

反応条件

温度100 °C

反応手順

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%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822518B2
出典データセットuspto-grants-2014_09
ORD IDord-1348729079e345cb9e93a57d7063f141
出典メモuspto-grants-2014_09