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Hydrochloric Acid → 1-(Pyridin-3-yl)piperazin-2-one

HRID 2213046
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HRID 2213046 반응식
O[CH2:2][CH2:3][NH:4][CH2:5][C:6]([NH:8][C:9]1[CH:10]=[N:11][CH:12]=[CH:13][CH:14]=1)=[O:7].C(P(CCCC)CCCC)CCC.Cl.C(N(CC)CC)C>O1CCCC1>[N:11]1[CH:12]=[CH:13][CH:14]=[C:9]([N:8]2[CH2:2][CH2:3][NH:4][CH2:5][C:6]2=[O:7])[CH:10]=1
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참가 물질

6

반응물 4

HCID 313Hydrochloric AcidHCID 8471TriethylamineHCID 13831TributylphosphineHCID 218650052-[(2-hydroxyethyl)amino]-N-(3-pyridinyl)acetamide

생성물 1

HCID 218650091-(Pyridin-3-yl)piperazin-2-one수율 35%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매
2회

실험 절차

Bis(1,1-dimethylethyl)diazenedicarboxylate (4.1 g, 18 mmol) in tetrahydrofuran (100 mL) was added dropwise to a stirred, cooled (0° C.) solution of 2-[(2-hydroxyethyl)amino]-N-(3-pyridinyl)acetamide (Description 142, 2.5 g, 13 mmol) and tributylphosphine (4.2 mL, 16.9 mmol) in tetrahydrofuran (300 mL) and the mixture was stirred at room temperature for 16 hours. Ethereal hydrogen chloride (1M, 10 mL) was added and the mixture was stirred at room temperature for 1 hour. Triethylamine (6 mL, 42 mmol) was added the solvent was evaporated under reduced pressure and the residue was purified by flash column chromatography on silica gel, eluting with CH2Cl2/MeOH/NH3(Aq.) (90:10:1), to give the title compound (800 mg, 35%). m/z (ES+) 178 (M+1).

후처리

  1. stirringthe mixture was stirred at room temperature for 1 hour
  2. customwas evaporated under reduced pressure
  3. customthe residue was purified by flash column chromatography on silica gel
  4. washeluting with CH2Cl2/MeOH/NH3(Aq.) (90:10:1)

출처 및 근거

ORD 기록
ord-01700779e19543c6b62083ede2d2f3fa
출처 데이터셋
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07105507B2

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