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3-Iodo-7-methoxy-2-phenyl-pyrano[2,3-b]pyridin-4-one → 3-Iodo-2-phenyl-8H-pyrano[2,3-b]pyridine-4,7-dione

HRID 1037246
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인쇄 미리보기

반응식

HRID 1037246 반응식
[I:1][C:2]1[C:3](=[O:20])[C:4]2[C:5]([O:12][C:13]=1[C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)=[N:6][C:7]([O:10]C)=[CH:8][CH:9]=2>Br.CC(O)=O>[I:1][C:2]1[C:3](=[O:20])[C:4]2[CH:9]=[CH:8][C:7](=[O:10])[NH:6][C:5]=2[O:12][C:13]=1[C:14]1[CH:15]=[CH:16][CH:17]=[CH:18][CH:19]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 670676803-Iodo-7-methoxy-2-phenyl-pyrano[2,3-b]pyridin-4-one

생성물 1

HCID 866710233-Iodo-2-phenyl-8H-pyrano[2,3-b]pyridine-4,7-dione

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 260Hydrogen Bromide용매

반응 조건

온도
60 °C

실험 절차

A suspension of 3-iodo-7-methoxy-2-phenyl-pyrano[2,3-b]pyridin-4-one (0.25 g, 0.66 mmol) in 33% hydrogen bromide solution in AcOH (3.5 mL) was heated in a microwave oven at 60° C. for 50 min. The resultant solution was evaporated to dryness. Toluene was added to the residual solid and evaporated. The orange solid was used without further purification. LCMS (Method B): RT=3.85 min, [M+H]+=366.

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. customThe resultant solution was evaporated to dryness
  2. additionToluene was added to the residual solid
  3. customevaporated
  4. customThe orange solid was used without further purification

출처 및 근거

ORD 기록
ord-4c0b62a6f66547669b62ab2b6c292b52
출처 데이터셋
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08546376B2

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