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

Sodium methanethiolate → 3-Pyridinecarboxamide, 5-mercapto-N,N-dimethyl-

HRID 230858
노트
인쇄 미리보기

반응식

HRID 230858 반응식
C[S-:2].[Na+].Br[C:5]1[CH:6]=[C:7]([C:11]([N:13]([CH3:15])[CH3:14])=[O:12])[CH:8]=[N:9][CH:10]=1>CN(C)C=O>[SH:2][C:5]1[CH:6]=[C:7]([C:11]([N:13]([CH3:15])[CH3:14])=[O:12])[CH:8]=[N:9][CH:10]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 4378561Sodium methanethiolateHCID 234370495-Bromo-N,N-dimethylpyridine-3-carboxamide

생성물 1

HCID 577631833-Pyridinecarboxamide, 5-mercapto-N,N-dimethyl-수율 90.5%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
100 °C

실험 절차

Sodium thiomethoxide (3 g) was added to a stirred solution of 5-bromo-N,N-dimethyl-3-pyridinecarboxamide (2.5g, WO2000055168) in N,N-dimethylformamide (40 ml) and the suspension stirred at 100° C. for 4 h. The solvent was concentrated in vacuo, the residue dissolved in 2M sodium hydroxide (35 ml) and water (50 ml), and the solution washed with chloroform (4×75 ml). The aqueous layer was acidified with 2M hydrochloric acid to pH 4 and extracted with chloroform (5×80 ml), and the combined organic layers were washed with brine (20 ml), dried over magnesium sulphate and concentrated in vacuo to give the title compound as an orange oil (1.8 g).

후처리

  1. concentrationThe solvent was concentrated in vacuo
  2. dissolutionthe residue dissolved in 2M sodium hydroxide (35 ml)
  3. washwater (50 ml), and the solution washed with chloroform (4×75 ml)
  4. extractionextracted with chloroform (5×80 ml)
  5. washthe combined organic layers were washed with brine (20 ml)
  6. dry with materialdried over magnesium sulphate
  7. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-a57ceb05a5074d88afd100135ff47684
출처 데이터셋
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07566786B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트