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Diphenyl Ether → 8-Bromo-7-methoxy-1,6-naphthyridin-4(1H)-one

HRID 1013629
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HRID 1013629 반응식
[Br:1][C:2]1[C:3]([O:20][CH3:21])=[N:4][CH:5]=[CH:6][C:7]=1[NH:8][CH:9]=[C:10]1[C:15](=[O:16])OC(C)(C)OC1=O.C1(OC2C=CC=CC=2)C=CC=CC=1>CCCCCC>[Br:1][C:2]1[C:3]([O:20][CH3:21])=[N:4][CH:5]=[C:6]2[C:7]=1[NH:8][CH:9]=[CH:10][C:15]2=[O:16]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 7583Diphenyl EtherHCID 673175935-[(3-Bromo-2-methoxy-pyridin-4-ylamino)-methylene]-2,2-dimethyl-[1,3]dioxane-4,6-dione

생성물 1

HCID 673185318-Bromo-7-methoxy-1,6-naphthyridin-4(1H)-one

시약·촉매·용매 1

HCID 8058Hexane용매2회

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온도
250 °C

실험 절차

A two neck RBF equipped with an air condenser was charged with 5-[(3-Bromo-2-methoxy-pyridin-4-ylamino)-methylene]-2,2-dimethyl-[1,3]dioxane-4,6-dione (23 g, 64 mmol) and diphenyl ether (230 mL). The reaction mixture was heated at 250° C. for 30 min under nitrogen atmosphere after which it was cooled to RT, diluted with hexane and filtered to obtain a dark solid. The crude product was refluxed in hexane for 30 min and filtered to obtained 8-Bromo-7-methoxy-1H-[1,6]naphthyridin-4-one as a brown solid.

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

후처리

  1. customA two neck RBF equipped with an air condenser
  2. temperaturewas cooled to RT
  3. filtrationfiltered
  4. customto obtain a dark solid
  5. filtrationfiltered

출처 및 근거

ORD 기록
ord-17e2973f69da4e5cb7e3d6bba9cfb109
출처 데이터셋
uspto-grants-2011_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07981891B2

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