Water → 3-[7-fluoro-4-propargyl-2H-1,4-benzoxazin-3(4H)-on-6-yl]-5-isopropylidene-1,3-oxazolidin-2,4-dione

HRID 1109719노트

반응식

HRID 1109719 반응식
[F:1][C:2]1[C:15]([N:16]=[C:17]=[O:18])=[CH:14][C:5]2[N:6]([CH2:11][C:12]#[CH:13])[C:7](=[O:10])[CH2:8][O:9][C:4]=2[CH:3]=1.[OH:19][CH:20]([C:25]([CH3:27])=[CH2:26])[C:21]([O:23]C)=O.C1CCN2C(=NCCC2)CC1.O>C1C=CC=CC=1>[F:1][C:2]1[C:15]([N:16]2[C:21](=[O:23])[C:20](=[C:25]([CH3:27])[CH3:26])[O:19][C:17]2=[O:18])=[CH:14][C:5]2[N:6]([CH2:11][C:12]#[CH:13])[C:7](=[O:10])[CH2:8][O:9][C:4]=2[CH:3]=1

참가 물질

6

실험 절차

To a solution of 7-fluoro-6-isocyanato-4-propargyl-2H-1,4-benzoxazin-3(4H)-one (2.5 g) and methyl 2-hydroxy-3-methyl-3-butenoate (1.3 g) in benzene (50 ml), DBU (1.5 g) was added at room temperature. The resulting mixture was refluxed for 10 hours, cooled to room temperature, combined with water and extracted with ethyl acetate. The organic layer was washed with water, dried over magnesium sulfate and concentrated. The residue was purified by silica gel column chromatography using a mixture of toluene and ethyl acetate as the eluent to give Compound No. 9 (3.0 g).

후처리

  1. temperatureThe resulting mixture was refluxed for 10 hours
  2. extractionextracted with ethyl acetate
  3. washThe organic layer was washed with water
  4. dry with materialdried over magnesium sulfate
  5. concentrationconcentrated
  6. customThe residue was purified by silica gel column chromatography
  7. additiona mixture of toluene and ethyl acetate as the eluent
  8. customto give Compound No

출처 및 근거

ORD 기록
ord-739631156dfb4d019882bfd3964d98a5
출처 데이터셋
uspto-grants-1994_06
특허 번호
US05322835

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