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2-(Methylamino)ethanol → HCID 57663183, 화합물

HRID 548653
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HRID 548653 반응식
CCN(C(C)C)C(C)C.F[C:11]1[C:19]([F:20])=[C:18]([F:21])[CH:17]=[CH:16][C:12]=1[C:13](Cl)=[O:14].[CH3:22][NH:23][CH2:24][CH2:25][OH:26].[H-].[Na+]>C(Cl)Cl.CO.O>[F:21][C:18]1[CH:17]=[CH:16][C:12]2[C:13](=[O:14])[N:23]([CH3:22])[CH2:24][CH2:25][O:26][C:11]=2[C:19]=1[F:20]
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참가 물질

8

반응물 4

HCID 80162-(Methylamino)ethanolHCID 24758Sodium hydrideHCID 81531DiisopropylethylamineHCID 27340222,3,4-Trifluorobenzoyl chloride

생성물 1

HCID 57663183HCID 57663183, 화합물수율 21.1%

시약·촉매·용매 3

HCID 887Methanol용매
HCID 962
Water
용매
HCID 6344Dichloromethane용매

실험 절차

DIPEA (0.68 mL, 3.9 mmol) was added to a solution of 2,3,4-trifluorobenzoyl chloride (500 mg, 2.6 mmol) in DCM (5 mL) followed by the addition of N-methylethanolamine (0.31 mL, 3.9 mmol). The mixture was stirred for 20 hours. The solution was diluted with methanol (10 mL) and passed through an ISOLUTE® SCX-2 SPE column. The solution was evaporated. The residue was dissolved in DMF and sodium hydride (60% dispersion in mineral oil, 0.11 g, 2.7 mmol) was added portionwise over 5 minutes. The resulting mixture was stirred for 20 hours. Water (100 mL) was added dropwise and the mixture was extracted with ether (3×200 mL). Combined ethereal extracts were dried (MgSO4) and evaporated. The residue was purified by column chromatography (eluting with 1:1 ethyl acetate:isohexane to neat ethyl acetate) to afford the title compound (117 mg, 20%) as a colourless solid.

후처리

  1. customThe solution was evaporated
  2. dissolutionThe residue was dissolved in DMF
  3. stirringThe resulting mixture was stirred for 20 hours
  4. extractionthe mixture was extracted with ether (3×200 mL)
  5. dry with materialwere dried (MgSO4)
  6. customevaporated
  7. customThe residue was purified by column chromatography (eluting with 1:1 ethyl acetate:isohexane to neat ethyl acetate)

출처 및 근거

ORD 기록
ord-b45d8d43704e422eb09e2c1f9e231196
출처 데이터셋
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07943607B2

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