5-hydroxy-4-propyldihydrofuran-2(3H)-one → HCID 15979801, 화합물

HRID 1924337노트

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HRID 1924337 반응식
[F:1][C:2]1[CH:3]=[C:4]2[N:9]([C:10]=1[CH2:11][NH2:12])[CH:8]=[CH:7][CH:6]=[CH:5]2.O[CH:14]1[O:18][C:17](=O)[CH2:16][CH:15]1[CH2:20][CH2:21][CH3:22]>ClCCCl.ClCCl>[F:1][C:2]1[CH:3]=[C:4]2[N:9]([C:10]=1[CH2:11][N:12]1[CH2:14][CH:15]([CH2:20][CH2:21][CH3:22])[CH2:16][C:17]1=[O:18])[CH:8]=[CH:7][CH:6]=[CH:5]2

참가 물질

5

실험 절차

A solution of 1-(2-fluoroindolizin-3-yl)methanamine x263 (0.38 g, 2.3 mmol) and 5-hydroxy-4-propyldihydrofuran-2(3H)-one x252 (0.33 g, 2.3 mmol) in DCE (12 ml) is kept at room temperature for 2 h, then STAB (0.74 g, 3.5 mmol) is added, and the mixture is stirred overnight. The reaction mixture is kept under stirring at 50° C. for 2 h, cooled to room temperature, and diluted with dichloromethane (10 ml). The mixture is washed with a 20% K2CO3 solution (2×15 ml), and the aqueous layer is washed with brine (25 ml), dried over anhydrous Na2SO4 and evaporated. The residue (0.60 g) is purified by chromatography on silica gel (gradient: chloroform to chloroform/methanol 50/1) to isolate a product of approximately 80% purity (0.162 g). This product is purified by chromatography on silicagel (hexane/ethyl acetate 5/2) to afford pure 1-[(2-fluoroindolizin-3-yl)methyl]-4-propylpyrrolidin-2-one 264 (0.126 g).

후처리

  1. additionSTAB (0.74 g, 3.5 mmol) is added
  2. stirringunder stirring at 50° C. for 2 h
  3. washThe mixture is washed with a 20% K2CO3 solution (2×15 ml)
  4. washthe aqueous layer is washed with brine (25 ml)
  5. dry with materialdried over anhydrous Na2SO4
  6. customevaporated
  7. customThe residue (0.60 g) is purified by chromatography on silica gel (gradient: chloroform to chloroform/methanol 50/1)
  8. customto isolate a product of approximately 80% purity (0.162 g)
  9. customThis product is purified by chromatography on silicagel (hexane/ethyl acetate 5/2)

출처 및 근거

ORD 기록
ord-e881bb617928405780b8f98f7e4ed9c1
출처 데이터셋
uspto-grants-2012_05
특허 번호
US08178533B2

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