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Pyridine-2-carbonitrile → Cqp4A25CE2

HRID 1171168
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HRID 1171168 반응식
[C:1]([C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][N:4]=1)#[N:2].O.[NH2:10][NH2:11]>CCO>[CH:7]1[CH:8]=[C:3](/[C:1](/[NH2:2])=[N:10]\[NH2:11])[N:4]=[CH:5][CH:6]=1
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참가 물질

4

반응물 2

HCID 7522Pyridine-2-carbonitrileHCID 24654Hydrazine hydrate (1:1)

생성물 1

HCID 5481389Cqp4A25CE2수율 137.5%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
0 °C

실험 절차

2-Cyano pyridine (500 mg, 1.923 mmol) and Hydrazine hydrate (252 mg, 1.923 mmol) were mixed together in EtOH (3 ml). The clear solution was left at 15° C. (in refrigerator) for 18 h (Monitored by TLC). Ethanol was concentrated under reduced pressure and then the reaction mixture was diluted with diethyl ether (50 ml) and water. The diethyl ether layer was separated, washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure to 1/5th Volume. The ethereal solution was cooled to 0° C. and the obtained solid precipitate was collected over the filtration and dried under vacuum, which gave the 2-pyridine Amidrazone (360 mg).

후처리

  1. concentrationEthanol was concentrated under reduced pressure
  2. additionthe reaction mixture was diluted with diethyl ether (50 ml) and water
  3. customThe diethyl ether layer was separated
  4. washwashed with brine
  5. dry with materialdried over Na2SO4
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure to 1/5th Volume
  8. filtrationthe obtained solid precipitate was collected over the filtration
  9. customdried under vacuum, which

출처 및 근거

ORD 기록
ord-69fecea4563a43a794e7340f3caa5c4e
출처 데이터셋
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07829589B2

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