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HRID 445275作成日:2026年10月26日

4-Nitrophenyl pyridin-2-ylcarbamate → (R)-N-(Pyridin-2-yl)-1-(4-(trifluoromethyl)phenyl)-3,4-dihydroisoquinoline-2(1H)-carboxamide

https://huagongshe.com/reaction/445275

反応式

関与物質

役割名称HCID仕込み量
反応物4-Nitrophenyl pyridin-2-ylcarbamateHCID 10332773—
反応物(R)-1-(4-(trifluoromethyl)phenyl)-1,2,3,4-tetrahydroisoquinolineHCID 28293305—
溶媒AcetonitrileHCID 6342—
生成物(R)-N-(Pyridin-2-yl)-1-(4-(trifluoromethyl)phenyl)-3,4-dihydroisoquinoline-2(1H)-carboxamideHCID 42635101—

反応条件

温度70 °C

反応手順

To a solution of (R)-1-(4-(trifluoromethyl)phenyl)-1,2,3,4-tetrahydroisoquinoline (100 mg, 0.361 mmol) in MeCN (2 mL) was added 4-nitrophenyl pyridin-2-ylcarbamate (467 mg, 1.80 mmol). The resulting mixture was then heated at 70° C. for 16 h, cooled to RT and filtered. The white solid obtained was washed with DCM (2×2 mL). The combined filtrates were then concentrated and the residue purified by silica gel flash column chromatography (0%-100% EtOAc/hexane) to give the title compound as a colorless solid. MS (ESI, positive ion) m/z: 398 (M+H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08476297B2
出典データセットuspto-grants-2013_07
ORD IDord-59df1fca6aae47fb8e7587a497fdab4b
出典メモuspto-grants-2013_07