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

Methyl iodide → 2-Amino-3-methyl-6-phenyl-4-pyrimidinone

HRID 1785440
노트
인쇄 미리보기

반응식

HRID 1785440 반응식
[OH-].[K+].[CH3:3]I.[NH2:5][C:6]1[NH:11][C:10](=[O:12])[CH:9]=[C:8]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=2)[N:7]=1>CCO>[NH2:5][C:6]1[N:11]([CH3:3])[C:10](=[O:12])[CH:9]=[C:8]([C:13]2[CH:14]=[CH:15][CH:16]=[CH:17][CH:18]=2)[N:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6328Methyl iodide2회HCID 14797Potassium HydroxideHCID 1354203652-Amino-6-phenylpyrimidin-4-ol

생성물 1

HCID 133205052-Amino-3-methyl-6-phenyl-4-pyrimidinone

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

A mixture of KOH (1.22 g, 22 mmol), MeI (6.85 g, 48 mmol), and 2-amino-6-phenyl-3H-pyrimidin-4-one (2.62 g, 14 mmol) in EtOH (130 mL) was stirred at room temperature in a stoppered 250 mL roundbottom flask for 3 days. An additional 6.85 g (48 mmol) MeI was added and stirring was continued for 1 day. The solvent was removed under vacuum and the residue was dissolved in H2O (35mL), warmed to 50° C., and 1N HCl was added dropwise until the solid dissolved completely. The solution was cooled to room temperature, made slightly basic with saturated NaHCO3, and the resulting white solid was filtered and dried under vacuum. M+1: 202.

후처리

  1. stirringstirring
  2. waitwas continued for 1 day
  3. customThe solvent was removed under vacuum
  4. dissolutionthe residue was dissolved in H2O (35mL)
  5. temperaturewarmed to 50° C.
  6. addition1N HCl was added dropwise until the solid
  7. dissolutiondissolved completely
  8. temperatureThe solution was cooled to room temperature
  9. filtrationthe resulting white solid was filtered
  10. customdried under vacuum

출처 및 근거

ORD 기록
ord-39cb08f716ea46fc9d7265a15ce12e7a
출처 데이터셋
uspto-grants-2009_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07504403B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트