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Water → Potassium 6-(4-ethyl-1-piperazinyl)pyridine-3-carboxylate

HRID 1003317
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HRID 1003317 반응식
[CH2:1]([N:3]1[CH2:8][CH2:7][N:6]([C:9]2[N:14]=[CH:13][C:12]([C:15]([O:17]CC)=[O:16])=[CH:11][CH:10]=2)[CH2:5][CH2:4]1)[CH3:2].[OH-].[K+:21].O.C(O)(C)C>CO>[CH2:1]([N:3]1[CH2:4][CH2:5][N:6]([C:9]2[N:14]=[CH:13][C:12]([C:15]([O-:17])=[O:16])=[CH:11][CH:10]=2)[CH2:7][CH2:8]1)[CH3:2].[K+:21]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 3776IsopropanolHCID 14797Potassium HydroxideHCID 18796410Ethyl 6-(4-ethyl-1-piperazinyl)pyridine-3-carboxylate

생성물 1

HCID 23663822Potassium 6-(4-ethyl-1-piperazinyl)pyridine-3-carboxylate수율 97.5%

시약·촉매·용매 1

HCID 887Methanol용매
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2회

실험 절차

To a solution of 69.81 g of ethyl 6-(4-ethyl-1-piperazinyl)pyridine-3-carboxylate in 280 ml of methanol were added 37 g of potassium hydroxide and a small volume of water and the mixture was heated under reflux for one hour. To the reaction solution were added methanol and isopropyl alcohol, the crystal thus precipitated out was recovered by filtration and then dried under reduced pressure to afford 70.65 g of the title compound as a colorless crystal.

후처리

  1. temperatureunder reflux for one hour
  2. customthe crystal thus precipitated out
  3. filtrationwas recovered by filtration
  4. customdried under reduced pressure

출처 및 근거

ORD 기록
ord-f2378e894660475cae36575a03adf7cf
출처 데이터셋
uspto-grants-2000_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06046201

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