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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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 4-Nitrophenyl pyridin-2-ylcarbamate | HCID 10332773 | — |
| 反応物 | (R)-1-(4-(trifluoromethyl)phenyl)-1,2,3,4-tetrahydroisoquinoline | HCID 28293305 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | (R)-N-(Pyridin-2-yl)-1-(4-(trifluoromethyl)phenyl)-3,4-dihydroisoquinoline-2(1H)-carboxamide | HCID 42635101 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08476297B2 |
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| 出典データセット | uspto-grants-2013_07 |
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| ORD ID | ord-59df1fca6aae47fb8e7587a497fdab4b |
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| 出典メモ | uspto-grants-2013_07 |
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