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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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4-Fluoroaniline → (R)-(4-fluoro-phenylamino)-phenyl-acetic acid methyl ester

HRID 77051
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인쇄 미리보기

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HRID 77051 반응식
CS(O[C@@H:6]([C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)[C:7]([O:9][CH3:10])=[O:8])(=O)=O.[F:17][C:18]1[CH:24]=[CH:23][C:21]([NH2:22])=[CH:20][CH:19]=1>CC#N>[CH3:10][O:9][C:7](=[O:8])[C@H:6]([NH:22][C:21]1[CH:23]=[CH:24][C:18]([F:17])=[CH:19][CH:20]=1)[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1
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참가 물질

4

반응물 2

HCID 97314-FluoroanilineHCID 10999262(S)-methyl 2-(methylsulfonyloxy)-2-phenylacetate

생성물 1

HCID 59401123(R)-(4-fluoro-phenylamino)-phenyl-acetic acid methyl ester수율 94.2%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

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온도
120 °C

실험 절차

To a solution of (S)-methyl 2-(methylsulfonyloxy)-2-phenylacetate (I5) (520 mg, 2.13 mmol) in CH3CN (10 mL), is added 4-fluoroaniline (473 mg, 4.26 mmol) and the mixture is heated at 120° C. for 5 minutes under MW irradiation (UPLC-MS: complete conversion). Acetonitrile was evaporated and the resulting crude is dissolved in 1N HCl and extracted several times with EtOAc. The combined organic phase is dried over Na2SO4, filtered and evaporated to dryness to obtain intermediate I254 as a pale yellow oil (520 mg, 94% yield).

후처리

  1. customAcetonitrile was evaporated
  2. dissolutionthe resulting crude is dissolved in 1N HCl
  3. extractionextracted several times with EtOAc
  4. dry with materialThe combined organic phase is dried over Na2SO4
  5. filtrationfiltered
  6. customevaporated to dryness

출처 및 근거

ORD 기록
ord-5d4cd55e8bcb4eba81382997411fbf1a
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08835682B2

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