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Hydrazine hydrate (1:1) → 2-[(3S)-1-(cyclopropylcarbonyl)-3-pyrrolidinyl]acetohydrazide

HRID 2405309
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HRID 2405309 반응식
[CH:1]1([C:4]([N:6]2[CH2:10][CH2:9][C@@H:8]([CH2:11][C:12]([O:14]CC)=O)[CH2:7]2)=[O:5])[CH2:3][CH2:2]1.O.[NH2:18][NH2:19]>C(O)C.ClCCl>[CH:1]1([C:4]([N:6]2[CH2:10][CH2:9][C@@H:8]([CH2:11][C:12]([NH:18][NH2:19])=[O:14])[CH2:7]2)=[O:5])[CH2:3][CH2:2]1
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참가 물질

5

반응물 2

HCID 24654Hydrazine hydrate (1:1)HCID 86674824ethyl [(3S)-1-(cyclopropylcarbonyl)-3-pyrrolidinyl]acetate

생성물 1

HCID 673540782-[(3S)-1-(cyclopropylcarbonyl)-3-pyrrolidinyl]acetohydrazide수율 100%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 6344Dichloromethane용매

반응 조건

온도
80 °C

실험 절차

In a round bottom flask equipped with reflux condenser, an orange solution of ethyl [(3S)-1-(cyclopropylcarbonyl)-3-pyrrolidinyl]acetate (56.1 g, 249 mmol) in ethanol (356 mL) was treated with hydrazine monohydrate (242 mL, 4.98 mol). The resultant yellow solution was stirred at 80° C. (reflux) for 15 h. The reaction was cooled to room temperature and concentrated in vacuo. Ethanol (100 mL) was added and the reaction was concentrated (2×) to give a pale yellow clear oil. The oil was dissolved in dichloromethane (white solution observed), dried over MgSO4, concentrated in vacuo, and pumped under high vacuum overnight (16 h) to give the title compound as a clear pale yellow oil (249 mmol, quantitative). MS(ES)+ m/e 212.0 [M+H]+, 423.2 [2M+H]+.

후처리

  1. customIn a round bottom flask equipped
  2. temperaturewith reflux condenser
  3. temperature(reflux) for 15 h
  4. temperatureThe reaction was cooled to room temperature
  5. concentrationconcentrated in vacuo
  6. additionEthanol (100 mL) was added
  7. concentrationthe reaction was concentrated (2×)
  8. customto give a pale yellow clear oil
  9. dry with materialdried over MgSO4
  10. concentrationconcentrated in vacuo
  11. custompumped under high vacuum overnight (16 h)

출처 및 근거

ORD 기록
ord-51807bdb7ac8468e97007e2f0bc8877e
출처 데이터셋
uspto-grants-2014_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08802864B2

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