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HRID 445277作成日:2026年10月24日

Carbamic acid, 4-pyridinyl-, 4-nitrophenyl ester → (R)-N-(Pyridin-4-yl)-1-(4-(trifluoromethyl)phenyl)-3,4-dihydroisoquinoline-2(1H)-carboxamide

https://huagongshe.com/ja/reaction/445277

反応式

関与物質

役割名称HCID仕込み量
反応物Carbamic acid, 4-pyridinyl-, 4-nitrophenyl esterHCID 10355188—
反応物(R)-1-(4-(trifluoromethyl)phenyl)-1,2,3,4-tetrahydroisoquinolineHCID 28293305—
溶媒AcetonitrileHCID 6342—
生成物(R)-N-(Pyridin-4-yl)-1-(4-(trifluoromethyl)phenyl)-3,4-dihydroisoquinoline-2(1H)-carboxamideHCID 59536398—

反応条件

温度55 °C

反応手順

To a solution of (R)-1-(4-(trifluoromethyl)phenyl)-1,2,3,4-tetrahydroisoquinoline (200 mg, 0.721 mmol) in MeCN (3 mL) was added 4-nitrophenyl pyridin-4-ylcarbamate (561 mg, 2.164 mmol). The resulting mixture was heated to 55° C. overnight. After cooling down to RT the white precipitated obtained was filtered off and washed with DCM (2×1 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 white 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-52b057d0de864447b934fff0ed6b9904
出典メモuspto-grants-2013_07