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Ethanolamine → 1-(2-Hydroxyethyl)-3,3-dimethylpiperazine-2,5-dione

HRID 1770734
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HRID 1770734 반응식
Cl[CH2:2][C:3]([NH:5][C:6]([CH3:12])([CH3:11])[C:7]([O:9]C)=O)=[O:4].[CH2:13]([CH2:15][NH2:16])[OH:14].C(N(CC)C(C)C)(C)C>O1CCCC1>[OH:14][CH2:13][CH2:15][N:16]1[CH2:2][C:3](=[O:4])[NH:5][C:6]([CH3:12])([CH3:11])[C:7]1=[O:9]
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참가 물질

5

반응물 3

HCID 700EthanolamineHCID 81531DiisopropylethylamineHCID 43700001HCID 43700001, 화합물

생성물 1

HCID 199580901-(2-Hydroxyethyl)-3,3-dimethylpiperazine-2,5-dione수율 42.3%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
155 °C

실험 절차

A solution of methyl 2-(2-chloroacetamido)-2-methylpropanoate (2.5 g, 13 mmol), ethanolamine (1.3 g, 21.3 mmol), and N,N-diisopropylethylamine (4.0 mL, 23 mmol) in 250 mL of anhydrous tetrahydrofuran was heated at reflux temperature for 24 hours. The mixture was concentrated to a residue in vacuo and dissolved in ethanol (approximately 300 mL). The mixture was heated in a sealed tube at 155° C. for 24 hours then concentrated to a crude residue and purified by column chromatography (5 to 12% methanol in dichloromethane) to give the title compound as a white solid (1.03 g, 5.5 mmol, 42%). 1H NMR (DMSO-d6, 400 MHz) δ 1.30 (s, 6H), 3.32-3.35 (t, J=5.7, 2H), 3.48-3.53 (q, J=5.7, 2H) 4.02 (s, 2H), 4.75-4.77 (t, J=5.4 Hz, 1H). LRMS (ESI/APCI) m/z 187 [M+H]+.

후처리

  1. temperatureat reflux temperature for 24 hours
  2. concentrationThe mixture was concentrated to a residue in vacuo
  3. dissolutiondissolved in ethanol (approximately 300 mL)
  4. concentrationthen concentrated to a crude residue
  5. custompurified by column chromatography (5 to 12% methanol in dichloromethane)

출처 및 근거

ORD 기록
ord-a34fe85e35af450e9f04129ab51de76e
출처 데이터셋
uspto-grants-2016_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09248117B2

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