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Diisopropylethylamine → HCID 178469923, 화합물

HRID 1753100
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HRID 1753100 반응식
Cl.[NH2:2][NH2:3].CCN(C(C)C)C(C)C.C(O/[CH:16]=[C:17](/[C:23](=O)[C:24]([F:27])([F:26])[F:25])\[C:18]([O:20][CH2:21][CH3:22])=[O:19])C>C(O)C>[CH2:21]([O:20][C:18]([C:17]1[C:23]([C:24]([F:27])([F:26])[F:25])=[N:2][NH:3][CH:16]=1)=[O:19])[CH3:22]
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참가 물질

5

반응물 3

HCID 81531DiisopropylethylamineHCID 115031Hydrazinium chlorideHCID 2737179Ethyl 2-(ethoxymethylene)-4,4,4-trifluoroacetoacetate

생성물 1

HCID 178469923HCID 178469923, 화합물수율 46.8%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

To a suspension of hydrazine hydrochloride (10 g, 146.66 mmol) in ethanol (500 mL) at −20° C. was added DIPEA (45.3 mL, 266.66 mmol) followed by stirring at this temperature for 10 minutes. Ethyl (2Z)-2-(ethoxymethylene)-4,4,4-trifluoro-3-oxobutanoate (Preparation 113, 32 g, 133.33 mmol) was added and the reaction stirred at room temperature for 18 hours. The reaction was concentrated in vacuo and diluted with EtOAc. The organic solution was washed with water, dried over sodium sulphate and concentrated in vacuo. The residue was purified using silica gel column chromatography eluting with 30% EtOAc in hexane to afford the title compound (13 g) that was taken directly on to the next step.

후처리

  1. stirringthe reaction stirred at room temperature for 18 hours
  2. concentrationThe reaction was concentrated in vacuo
  3. additiondiluted with EtOAc
  4. washThe organic solution was washed with water
  5. dry with materialdried over sodium sulphate
  6. concentrationconcentrated in vacuo
  7. customThe residue was purified
  8. washeluting with 30% EtOAc in hexane

출처 및 근거

ORD 기록
ord-3563c8f4a88e4bf4ac0c080521875824
출처 데이터셋
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09163021B2

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