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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Acetic Acid → 4-(2-Acetylamino-4,5-difluorophenyl)butanoic acid

HRID 2257875
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인쇄 미리보기

반응식

HRID 2257875 반응식
[F:1][C:2]1[C:7]([F:8])=[CH:6][C:5]([CH2:9][CH2:10][CH2:11][C:12]([OH:14])=[O:13])=[C:4]([N+:15]([O-])=O)[CH:3]=1.[C:18](O)(=[O:20])[CH3:19]>C(OC(=O)C)(=O)C.[Pd]>[C:18]([NH:15][C:4]1[CH:3]=[C:2]([F:1])[C:7]([F:8])=[CH:6][C:5]=1[CH2:9][CH2:10][CH2:11][C:12]([OH:14])=[O:13])(=[O:20])[CH3:19]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 176Acetic AcidHCID 22449552HCID 22449552, 화합물

생성물 1

HCID 105872254-(2-Acetylamino-4,5-difluorophenyl)butanoic acid

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 7918Acetic Anhydride용매

실험 절차

The compound obtained in (3) above (380 mg) was dissolved in a mixed solvent of 5 ml of acetic acid and 10 ml of acetic anhydride. Upon the addition of 60 mg of 10% palladium-on-carbon, the mixture was catalytically hydrogenated. The catalyst was removed by filtration, the solvent was evaporated, and the residue was subjected to silica gel column chromatography using a chloroform-methanol (10:1) mixed solvent as an eluant to obtain fractions containing the target compound. The fractions were concentrated to produce 90 mg of the title compound.

후처리

  1. customThe catalyst was removed by filtration
  2. customthe solvent was evaporated
  3. additionmixed solvent as an eluant
  4. customto obtain fractions
  5. additioncontaining the target compound
  6. concentrationThe fractions were concentrated

출처 및 근거

ORD 기록
ord-5776a9c4cba146c2bc4ed203248acd13
출처 데이터셋
uspto-grants-1997_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05658920

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