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

Iodine → Methyl 6-amino-5-iodo-2-(methyloxy)-3-pyridinecarboxylate

HRID 489804
노트
인쇄 미리보기

반응식

HRID 489804 반응식
[NH2:1][C:2]1[N:7]=[C:6]([O:8][CH3:9])[C:5]([C:10]([O:12][CH3:13])=[O:11])=[CH:4][CH:3]=1.[I:14]I.O>CN(C)C=O.C(OCC)C>[NH2:1][C:2]1[N:7]=[C:6]([O:8][CH3:9])[C:5]([C:10]([O:12][CH3:13])=[O:11])=[CH:4][C:3]=1[I:14]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 807IodineHCID 962WaterHCID 11159681Methyl 6-amino-2-methoxynicotinate

생성물 1

HCID 22262635Methyl 6-amino-5-iodo-2-(methyloxy)-3-pyridinecarboxylate수율 79.8%

시약·촉매·용매 2

HCID 3283Diethyl Ether용매HCID 6228Dimethylformamide용매
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

실험 절차

A mixture of methyl 6-amino-2-(methyloxy)-3-pyridinecarboxylate (2.1 g, 11.8 mmol) and iodine (15 g, 59 mmol) in N,N-dimethylformamide (50 ml) was stirred overnight at room temperature. The mixture was poured into water (200 ml) and extracted with ethyl acetate (50 ml×2). The combined organic layer was washed with saturated sodium bicarbonate, 20% aqueous thiosulphate and brine, dried over magnesium sulfate, and concentrated in vacuo gave a brown solid. The residue was suspended in diethyl ether and collected by filtration to afford 2.9 g (79%) of the title compound as a pale brown solid.

후처리

  1. extractionextracted with ethyl acetate (50 ml×2)
  2. washThe combined organic layer was washed with saturated sodium bicarbonate, 20% aqueous thiosulphate and brine
  3. dry with materialdried over magnesium sulfate
  4. concentrationconcentrated in vacuo
  5. customgave a brown solid
  6. filtrationcollected by filtration

출처 및 근거

ORD 기록
ord-04f8aaed5660453993c189703e027da9
출처 데이터셋
uspto-grants-2005_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06979690B2

반응 노트

불러오는 중…