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Potassium Hydroxide → HCID 178437279, 화합물

HRID 256318
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HRID 256318 반응식
[CH2:1]([C:3]1[C:4]([O:15][CH3:16])=[N:5][C:6]2[N:7]([CH:10]=[C:11]([C:13]#[N:14])[N:12]=2)[C:8]=1[CH3:9])[CH3:2].Cl.[NH2:18][OH:19].[OH-].[K+]>C(O)C>[CH2:1]([C:3]1[C:4]([O:15][CH3:16])=[N:5][C:6]2[N:7]([CH:10]=[C:11]([C:13]([NH:18][OH:19])=[NH:14])[N:12]=2)[C:8]=1[CH3:9])[CH3:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 14797Potassium HydroxideHCID 443297Hydroxyamine hydrochlorideHCID 13669915HCID 13669915, 화합물

생성물 1

HCID 178437279HCID 178437279, 화합물수율 86.3%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A suspension of 8.0 g of 6-ethyl-7-methoxy-5-methylimidazo [1,2-a]pyrimidine-2-carbonitrile, 2.82 g of hydroxylamine hydrochloride and 2.28 g of potassium hydroxide in 100 ml of ethanol was refluxed with stirring for 2 hours and the mixture was cooled. The precipitated product was filtered, suspended in water with stirring for 15 minutes, filtered, then washed with water and ether and dried under vacuum to give 7.96 g of 6-ethyl-N-hydroxy-7-methoxy-5-methylimidazo[1,2-a]pyrimidine-2-carboxamidine (86% yield) melting at 249°-250° C.

후처리

  1. temperaturewas refluxed
  2. temperaturethe mixture was cooled
  3. filtrationThe precipitated product was filtered
  4. stirringwith stirring for 15 minutes
  5. filtrationfiltered
  6. washwashed with water and ether
  7. customdried under vacuum

출처 및 근거

ORD 기록
ord-fddb43ff183146cd865b9813271ea6b3
출처 데이터셋
uspto-grants-1987_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04703049

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