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Water → 4-chloro-7-fluoro-1H-indole-2-carboxylic acid ethyl ester

HRID 853064
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HRID 853064 반응식
C(OC(=O)C(=N[NH:8][C:9]1[CH:14]=[C:13]([Cl:15])[CH:12]=[CH:11][C:10]=1[F:16])C)C.[C:18]1(C)C=CC(S(O)(=O)=O)=C[CH:19]=1.O.[C:30](=[O:33])(O)[O-:31].[Na+].[C:35]1(C)C=CC=C[CH:36]=1>>[CH2:35]([O:31][C:30]([C:18]1[NH:8][C:9]2[C:14]([CH:19]=1)=[C:13]([Cl:15])[CH:12]=[CH:11][C:10]=2[F:16])=[O:33])[CH3:36]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 5

HCID 962WaterHCID 1140TolueneHCID 6101p-Toluenesulfonic acidHCID 516892Sodium BicarbonateHCID 865847132-[(5-Chloro-2-fluoro-phenyl)-hydrazono]-propionic acid ethyl ester

생성물 1

HCID 694157714-chloro-7-fluoro-1H-indole-2-carboxylic acid ethyl ester수율 23%

실험 절차

2-[(5-Chloro-2-fluoro-phenyl)-hydrazono]-propionic acid ethyl ester (13.2 g, 51 mmol) was dissolved in toluene, p-toluenesulfonic acid (10 g, 51 mmol) was added and the mixture was heated to reflux for 24 h with separation of water. The mixture was cooled, neutralized with saturated sodium bicarbonate (400 mL) and extracted thrice with ethyl acetate. Organic phases were pooled, washed with brine, dried with MgSO4 and the solvent was removed in vacuo. The residue was triturated with hexane to yield the title product as yellowish solid (2.9 g, 23%); EI-MS: m/e=241.1 (M+).

후처리

  1. temperaturethe mixture was heated
  2. temperatureThe mixture was cooled
  3. extractionextracted thrice with ethyl acetate
  4. washwashed with brine
  5. dry with materialdried with MgSO4
  6. customthe solvent was removed in vacuo
  7. customThe residue was triturated with hexane

출처 및 근거

ORD 기록
ord-5199bc7cef8d4b5599e0af3edca56b8d
출처 데이터셋
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07253281B2

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