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(4-Fluoro-2-nitro-phenylamino)-acetic acid → 7-Fluoro-1,2,3,4-tetrahydroquinoxalin-2-one

HRID 2279298
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HRID 2279298 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([NH:8][CH2:9][C:10](O)=[O:11])=[C:4]([N+:13]([O-])=O)[CH:3]=1>C(O)(=O)C.C(OCC)(=O)C.[Fe]>[F:1][C:2]1[CH:3]=[C:4]2[C:5]([NH:8][CH2:9][C:10](=[O:11])[NH:13]2)=[CH:6][CH:7]=1
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참가 물질

5

반응물 1

HCID 23337266(4-Fluoro-2-nitro-phenylamino)-acetic acid

생성물 1

HCID 229129097-Fluoro-1,2,3,4-tetrahydroquinoxalin-2-one수율 103.1%

시약·촉매·용매 3

HCID 23925Iron촉매HCID 176Acetic Acid용매HCID 8857Ethyl Acetate용매2회

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온도
90 °C

실험 절차

Iron powder (6.52 g, 116.8 mmol, 5.0 eq) is added at room temperature to a stirred solution of (4-fluoro-2-nitro-phenylamino)-acetic acid (6.85 g, 23.4 mmol, 1.0 eq) in glacial acetic acid (40 mL). The resulting suspension is heated at 90° C. for 3 hours, then cooled to room temperature, diluted with ethyl acetate (40 mL), and filtered through silica gel. The filtrate is concentrated to give a crude that is purified by column chromatography (silica gel, eluent: ethyl acetate:petroleum ether, 1:3, v/v) to afford 7-fluoro-3,4-dihydro-1H-quinoxalin-2-one as a brown solid (4.01 g, 72% yield).

후처리

  1. temperaturecooled to room temperature
  2. filtrationfiltered through silica gel
  3. concentrationThe filtrate is concentrated
  4. customto give a crude that
  5. customis purified by column chromatography (silica gel, eluent

출처 및 근거

ORD 기록
ord-6e37c729153145f49e58ee264453dbb2
출처 데이터셋
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09133219B2

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