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Ethanol → 2,5,7-Triazaspiro[3.4]octane-6,8-dione

HRID 2273021
노트
인쇄 미리보기

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HRID 2273021 반응식
C(OC([N:8]1[CH2:11][C:10](=O)[CH2:9]1)=O)(C)(C)C.[C-]#N.[K+].[C:16](=[O:19])([O-])[O-].[NH4+:20].[NH4+:21].[CH2:22]([OH:24])C>O>[CH2:11]1[C:10]2([NH:21][C:22](=[O:24])[NH:20][C:16]2=[O:19])[CH2:9][NH:8]1
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참가 물질

6

반응물 4

HCID 702EthanolHCID 9032Potassium CyanideHCID 517111Ammonium CarbonateHCID 15194043-Oxo-azetidine-1-carboxylic acid tert-butyl ester

생성물 1

HCID 666007202,5,7-Triazaspiro[3.4]octane-6,8-dione

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
90 °C

실험 절차

3-Oxo-azetidine-1-carboxylic acid tert-butyl ester (1 eq.) and potassium cyanide (1.3 eq) are dissolved in ethanol before ammonium carbonate (8 eq.) in water is added. The mixture is heated to 90° C. for 19 h and monitored by LCMS. Upon completion, the solvent is removed in vacuum. The residue is diluted with water and the product filtered off. Boc-deprotection under standard conditions gives the desired hydantoine as HCl-salt ready for further modifications.

후처리

  1. additionis added
  2. customUpon completion, the solvent is removed in vacuum
  3. additionThe residue is diluted with water
  4. filtrationthe product filtered off

출처 및 근거

ORD 기록
ord-350c788c2115403eb7d378c904a62964
출처 데이터셋
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09120804B2

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