Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 411515생성일: 2026년 10월 26일
Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate → (R)-1-[[2-(3,4-difluoroPhenyl)-4-quinoliny]carbonyl]-2-hydroxymethyl-pyrrolidine
https://huagongshe.com/reaction/411515
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | 2-(3,4-Difluorophenyl)-4-quinolinecarboxylic acid | HCID 4611633 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | (R)-1-[[2-(3,4-difluoroPhenyl)-4-quinoliny]carbonyl]-2-hydroxymethyl-pyrrolidine | HCID 9799393 | — |
반응 단계
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.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06559163B2 |
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| 출처 데이터셋 | uspto-grants-2003_05 |
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| ORD ID | ord-c38a426b38c0429fab38b282dfe34620 |
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| 출처 메모 | uspto-grants-2003_05 |
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