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HRID 594390作成日:2026年10月26日
N-([1,1'-biphenyl]-3-ylmethyl)-N-(1-(4-fluoro-2,6-dimethoxyphenyl)but-3-en-1-yl)acrylamide → 1-([1,1'-biphenyl]-3-ylmethyl)-6-(4-fluoro-2,6-dimethoxyphenyl)-5,6-dihydropyridin-2(1H)-one
https://huagongshe.com/reaction/594390
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | N-([1,1'-biphenyl]-3-ylmethyl)-N-(1-(4-fluoro-2,6-dimethoxyphenyl)but-3-en-1-yl)acrylamide | HCID 86695632 | — |
| 触媒 | Titanium isopropoxide | HCID 11026 | — |
| 触媒 | Benzylidenebis(tricyclohexylphosphine)dichlororuthenium | HCID 11967259 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 1-([1,1'-biphenyl]-3-ylmethyl)-6-(4-fluoro-2,6-dimethoxyphenyl)-5,6-dihydropyridin-2(1H)-one | HCID 69085596 | — |
反応手順
A yellow solution of N-([1,1′-biphenyl]-3-ylmethyl)-N-(1-(4-fluoro-2,6-dimethoxyphenyl)but-3-en-1-yl)acrylamide (152 mg; 0.34 mmol; 1.0 equiv.) in anh. DCM (17 ml) was treated with titanium(IV) isopropoxide (0.20 ml; 0.68 mmol; 2.0 equiv.), and the mixture was heated to 50° C., under nitrogen, for 1 h. Benzylidene-bis(tricyclohexylphosphine)dichlororuthenium (11.3 mg; 0.04 equiv.) was then added, and the resulting mixture was further heated at reflux for 20 h. Subsequent concentration to dryness under reduced pressure, and purification by FC (DCM/MeOH=50/1) afforded 1-([1,1′-biphenyl]-3-ylmethyl)-6-(4-fluoro-2,6-dimethoxyphenyl)-5,6-dihydropyridin-2(1H)-one as a pale yellow foam. LC-MS (conditions A): tR=0.94 min.; [M+H]+: 417.76 g/mol.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09242970B2 |
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| 出典データセット | uspto-grants-2016_01 |
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| ORD ID | ord-37b5b24d9c8e436b8e9f4d1f2ea4c121 |
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| 出典メモ | uspto-grants-2016_01 |
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