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

Sodium methanethiolate → 6-Methylsulfanyl-[2,3']bipyridin-3-ol

HRID 228806
노트
인쇄 미리보기

반응식

HRID 228806 반응식
F[C:2]1[N:7]=[C:6]([C:8]2[CH:9]=[N:10][CH:11]=[CH:12][CH:13]=2)[C:5]([O:14]C)=[CH:4][CH:3]=1.[CH3:16][S-:17].[Na+]>CN(C)C=O>[CH3:16][S:17][C:2]1[N:7]=[C:6]([C:8]2[CH:9]=[N:10][CH:11]=[CH:12][CH:13]=2)[C:5]([OH:14])=[CH:4][CH:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 4378561Sodium methanethiolateHCID 688289086-Fluoro-3-methoxy-[2,3']bipyridine

생성물 1

HCID 688293916-Methylsulfanyl-[2,3']bipyridin-3-ol수율 45%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
160 °C

실험 절차

6-Fluoro-3-methoxy-[2,3′]bipyridine (30 mg) and sodium thiomethoxide (103 mg) were suspended in N,N-dimethylformamide (1.5 ml), and the suspension was stirred at 160° C. for 4 hr. The reaction solution was cooled to room temperature, the reaction solution was filtered, and the solvent was removed from the filtrate by distillation under the reduced pressure. The residue was purified by thin layer chromatography using chloroform-methanol to give 6-methylsulfanyl-[2,3′]bipyridin-3-ol (13 mg, yield 45%).

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. temperatureThe reaction solution was cooled to room temperature
  2. filtrationthe reaction solution was filtered
  3. customthe solvent was removed from the filtrate by distillation under the reduced pressure
  4. customThe residue was purified by thin layer chromatography

출처 및 근거

ORD 기록
ord-2ef3d7694a8d4bcab706b166e0ceb66a
출처 데이터셋
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07560558B2

반응 노트

불러오는 중…