홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

6-Amino-3-methyl-2-methylsulfanyl-5-nitrosopyrimidin-4-one → 5,6-Diamino-3-methyl-2-(methylthio)pyrimidin-4(3H)-one

HRID 976947
노트
인쇄 미리보기

반응식

HRID 976947 반응식
[NH2:1][C:2]1[N:7]=[C:6]([S:8][CH3:9])[N:5]([CH3:10])[C:4](=[O:11])[C:3]=1[N:12]=O>[NH4+]=S>[NH2:12][C:3]1[C:4](=[O:11])[N:5]([CH3:10])[C:6]([S:8][CH3:9])=[N:7][C:2]=1[NH2:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

2

반응물 1

HCID 43919196-Amino-3-methyl-2-methylsulfanyl-5-nitrosopyrimidin-4-one

생성물 1

HCID 1816055,6-Diamino-3-methyl-2-(methylthio)pyrimidin-4(3H)-one

실험 절차

To 4.0 g (0.02 mole) of 6-amino-3-methyl-2-methylthio-5-nitroso-pyrimidine-4-one (44) was added 40 mL of 20% aqueous ammonium sulfide solution. The mixture was heated under reflux for 30 min. After cooling the precipitate was collected, washed with a little ethanol and dried in a desiccator to give 45 as 2.72 g (75% yield) of colorless crystals (m.p. 211°-212° C.).

후처리

  1. temperatureThe mixture was heated
  2. temperatureunder reflux for 30 min
  3. temperatureAfter cooling the precipitate
  4. customwas collected
  5. washwashed with a little ethanol
  6. customdried in a desiccator

출처 및 근거

ORD 기록
ord-04ca4354890e41f89c29f6bc0da8aba2
출처 데이터셋
uspto-grants-1997_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05612468

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트