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Keto-pantoyllactone → 3,4-diamino-6-(1',1'-dimethyl-2'-hydroxyethyl)-1,2,4,-triazin-5(4H)-one hydrochloride

HRID 843608
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HRID 843608 반응식
[CH3:1][C:2]1([CH3:9])[CH2:6][O:5][C:4](=[O:7])[C:3]1=O.[ClH:10].[NH2:11][NH:12][C:13]([NH:15][NH2:16])=[NH:14].O>C(O)C>[ClH:10].[NH2:14][C:13]1[N:15]([NH2:16])[C:4](=[O:7])[C:3]([C:2]([CH3:9])([CH3:1])[CH2:6][OH:5])=[N:11][N:12]=1
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참가 물질

5

반응물 3

HCID 39Keto-pantoyllactoneHCID 962WaterHCID 178479531HCID 178479531, 화합물

생성물 1

HCID 226111153,4-diamino-6-(1',1'-dimethyl-2'-hydroxyethyl)-1,2,4,-triazin-5(4H)-one hydrochloride수율 61%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Dihydro-4,4-dimethyl-2,3-furandione (2 g, 15.6 mmole) and 1,3-diaminoguanidine monohydrochloride (12.96 g, 15.61 mmole) were dissolved in ethanol and the resulting solution heated to reflux temperatures. To the refluxing reaction mixture, was added water until a clear solution was obtained. The mixture was then refluxed overnight, cooled to room temperature and stored at −20° C. overnight. The product which separated was filtered and dried. It was crystallized from a mixture of ethanol and water to give 3,4-diamino-6-(1′,1′-dimethyl-2′-hydroxyethyl)-1,2,4-triazin-5(4H)-one hydrochloride (2.24 g, 61%), m.p. 221-222° C. (dec).

후처리

  1. temperaturethe resulting solution heated
  2. temperatureto reflux temperatures
  3. customTo the refluxing reaction mixture
  4. customwas obtained
  5. temperatureThe mixture was then refluxed overnight
  6. customThe product which separated
  7. filtrationwas filtered
  8. customdried
  9. customIt was crystallized from a mixture of ethanol and water

출처 및 근거

ORD 기록
ord-862067304a844252aa24074a14206b26
출처 데이터셋
uspto-grants-2002_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06380192B1

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