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

Hydrochloric Acid → 1,6-Dihydro-4-hydroxy-1-methyl-2-methoxy-6-oxo-pyrimidine

HRID 261788
노트
인쇄 미리보기

반응식

HRID 261788 반응식
[OH:1][C:2]1[N:3]=[C:4](SC)[N:5]([CH3:9])[C:6](=[O:8])[CH:7]=1.[CH3:12][OH:13].Cl>CCOCC>[OH:1][C:2]1[N:3]=[C:4]([O:13][CH3:12])[N:5]([CH3:9])[C:6](=[O:8])[CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 313Hydrochloric AcidHCID 887MethanolHCID 1354085986-Hydroxy-1-methyl-2-(methylsulfanyl)pyrimidin-4(1h)-one

생성물 1

HCID 1358484661,6-Dihydro-4-hydroxy-1-methyl-2-methoxy-6-oxo-pyrimidine수율 40%

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

A mixture of 172 g (1 mol) of 1,6-dihydro-4-hydroxy-1-methyl-2-methylthio-6-oxo-pyrimidine, 700 ml of methanol and 5 ml of a solution of hydrogen chloride in ether was boiled for 10 days under reflux. The reaction mixture was then filtered while still hot and the filtrate is evaporated in vacuo. The residue was triturated with ether and the crystalline product was filtered off. In this way, 71 g (40% of theory) of 1,6-dihydro-4-hydroxy-1-methyl-2-methoxy-6-oxo-pyrimidine were obtained in the form of colorless crystals of melting point 170°-171° C. ##STR11##

후처리

  1. temperatureunder reflux
  2. filtrationThe reaction mixture was then filtered while still hot and the filtrate
  3. customis evaporated in vacuo
  4. customThe residue was triturated with ether
  5. filtrationthe crystalline product was filtered off

출처 및 근거

ORD 기록
ord-be41bb75b42b464f9fa7713bb4e877ed
출처 데이터셋
uspto-grants-1979_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04152426

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트