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Hydrochloric Acid → 5-Chloro-6-(3-nitro-1,2,4-triazol-1-ylmethyl)uracil

HRID 1600001
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인쇄 미리보기

반응식

HRID 1600001 반응식
[N+:1]([C:4]1[N:8]=[CH:7][NH:6][N:5]=1)([O-:3])=[O:2].[Cl:9][C:10]1[C:11](=[O:19])[NH:12][C:13](=[O:18])[NH:14][C:15]=1[CH2:16]Cl.Cl>[OH-].[K+]>[Cl:9][C:10]1[C:11](=[O:19])[NH:12][C:13](=[O:18])[NH:14][C:15]=1[CH2:16][N:6]1[CH:7]=[N:8][C:4]([N+:1]([O-:3])=[O:2])=[N:5]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 41710565-Chloro-6-(chloromethyl)-1,2,3,4-tetrahydropyrimidine-2,4-dioneHCID 178526901HCID 178526901, 화합물

생성물 1

HCID 216993145-Chloro-6-(3-nitro-1,2,4-triazol-1-ylmethyl)uracil수율 73%

시약·촉매·용매 1

HCID 14797Potassium Hydroxide용매

반응 조건

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트
온도
80 °C

실험 절차

To a solution of 0.88 g of 3-nitro-1,2,4-triazole in a 1N aqueous solution of KOH (10 ml), 0.50 g of 5-chloro-6-chloromethyluracil was added, followed by heating at 80° C. for 2.5 hours under stirring. The reaction mixture was neutralized with 6N hydrochloric acid. A precipitate was collected by filtration and then washed with water and methanol, whereby 510 mg of the title compound were obtained (yield: 73%).

후처리

  1. filtrationA precipitate was collected by filtration
  2. washwashed with water and methanol

출처 및 근거

ORD 기록
ord-c0258bda9546402b8f8917df235714fe
출처 데이터셋
uspto-grants-1998_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05744475

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