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Carbostyril, 3,4-dihydro-7-fluoro- → 7-Fluoro-1,2,3,4-tetrahydroquinoline

HRID 1520183
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HRID 1520183 반응식
[F:1][C:2]1[CH:11]=[C:10]2[C:5]([CH2:6][CH2:7][C:8](=O)[NH:9]2)=[CH:4][CH:3]=1>O1CCCC1>[F:1][C:2]1[CH:11]=[C:10]2[C:5]([CH2:6][CH2:7][CH2:8][NH:9]2)=[CH:4][CH:3]=1
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참가 물질

3

반응물 1

HCID 138300Carbostyril, 3,4-dihydro-7-fluoro-

생성물 1

HCID 162443877-Fluoro-1,2,3,4-tetrahydroquinoline수율 66%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매2회

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온도
60 °C

실험 절차

To a solution of 7-fluoro-1,2,3,4-tetrahydroquinolin-2-one (1.5 g, 9.08 mmol) in tetrahydrofuran (50 ml) was dropwise BH3 in THF (1M, 90 ml), the solution was stirred for 24 h at 60° C. The reaction mixture was cooled and then quenched by the addition of methanol (15 ml) and HCl (conc) (5 ml), then stirred for 1 h at 60° C. The reaction mixture was cooled to room temperature and adjusted to pH 12 with sodium hydroxide (4 mol/L), extracted with (3×15 ml) of ethyl acetate and the organic layers were combined and dried over anhydrous magnesium sulfate, concentrated in vacuo to give a residue, which was purified by a silica gel column chromatography with 3% ethyl acetate in petroleum ether to afford 7-fluoro-1,2,3,4-tetrahydroquinoline as a yellow solid (0.9 g, 66%).

후처리

  1. temperatureThe reaction mixture was cooled
  2. customquenched by the addition of methanol (15 ml) and HCl (conc) (5 ml)
  3. stirringstirred for 1 h at 60° C
  4. temperatureThe reaction mixture was cooled to room temperature
  5. extractionextracted with (3×15 ml) of ethyl acetate
  6. dry with materialdried over anhydrous magnesium sulfate
  7. concentrationconcentrated in vacuo
  8. customto give a residue, which
  9. customwas purified by a silica gel column chromatography with 3% ethyl acetate in petroleum ether

출처 및 근거

ORD 기록
ord-62e49abe3e214110ab49d4652556d06d
출처 데이터셋
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09073902B2

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