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HRID 411515作成日:2026年10月26日
Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate → (R)-1-[[2-(3,4-difluoroPhenyl)-4-quinoliny]carbonyl]-2-hydroxymethyl-pyrrolidine
https://huagongshe.com/reaction/411515
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| 反応物 | Sodium Bicarbonate | HCID 516892 | — |
| 反応物 | 2-(3,4-Difluorophenyl)-4-quinolinecarboxylic acid | HCID 4611633 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | (R)-1-[[2-(3,4-difluoroPhenyl)-4-quinoliny]carbonyl]-2-hydroxymethyl-pyrrolidine | HCID 9799393 | — |
反応手順
A mixture of 2-(3,4-difluoroPhenyl)-4-quinoline carboxylic acid (100 mg), BOP (220 mg) and (R)-(−)-pyrrolidine methanol (0.1 mL) in 1 ml of DMF is stirred at room temperature for 18 hours. The mixture is added to saturated aqueous NaHCO3 solution and extracted three times with EtOAc. The combined EtOAc layers are washed with brine and water, dried over Na2SO4, filtered and concentrated to afford a foam. The foam is purified by preparative silica gel thin layer chromatography, using 10% methanol in methylene chloride as the developing solvent. The desired product is obtained as a free base. 1H NMR (CDCl3) d 1.77 -1.87(3H, m), 2.16-2.22 (1H, m), 3.18-3.26 (2H, m), 3.83-3.95 (2H, m), 4.52-4.56 (1H, m), 7.23-7.30 (1H, m), 7.57 (1H, m), 7.73-7.78 (2H, m), 7.83 (1H, d), 7.87 (1H, m), 8.03-8.10 (1H, m), 8.15 (1H, d). The hydrochloride salt was prepared by treating the free base in EtOAc with a solution of hydrogen chloride in ether and collecting the resulting solid by filtration.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06559163B2 |
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| 出典データセット | uspto-grants-2003_05 |
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| ORD ID | ord-c38a426b38c0429fab38b282dfe34620 |
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| 出典メモ | uspto-grants-2003_05 |
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