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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 22030610, 화합물 → HCID 135763121, 화합물

HRID 454194
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반응식

HRID 454194 반응식
C([O:8][C:9]1[CH:18]=[C:17]2[C:12]([C:13]([O:19][C:20]3[CH:29]=[C:28]4[C:23]([CH:24]=[CH:25][CH:26]=[N:27]4)=[CH:22][CH:21]=3)=[N:14][CH:15]=[N:16]2)=[CH:11][C:10]=1[O:30][CH3:31])C1C=CC=CC=1>FC(F)(F)C(O)=O>[OH:8][C:9]1[CH:18]=[C:17]2[C:12]([C:13]([O:19][C:20]3[CH:29]=[C:28]4[C:23]([CH:24]=[CH:25][CH:26]=[N:27]4)=[CH:22][CH:21]=3)=[N:14][CH:15]=[N:16]2)=[CH:11][C:10]=1[O:30][CH3:31]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 22030610HCID 22030610, 화합물

생성물 1

HCID 135763121HCID 135763121, 화합물수율 76.2%

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

실험 절차

A solution of 7-benzyloxy-6-methoxy-4-(quinolin-7-yloxy)quinazoline (1.50 g, 3.70 mmol), (prepared as described in Example 196), in trifluoroacetic acid (50 ml) was heated at reflux for 150 minutes. The reaction was concentrated in vacuo and the reaction neutralised with saturated aqueous ammonium hydroxide. The resulting precipitate was filtered, washed with acetone and dried under suction to give 7-hydroxy-6-methoxy-4-(quinolin-7-yloxy)quinazoline (0.90 g, 2.82 mmol, 76%) as a white solid.

후처리

  1. temperatureat reflux for 150 minutes
  2. concentrationThe reaction was concentrated in vacuo
  • customthe reaction neutralised with saturated aqueous ammonium hydroxide
  • filtrationThe resulting precipitate was filtered
  • washwashed with acetone
  • customdried under suction
  • 출처 및 근거

    ORD 기록
    ord-e5804af195634958a281f83bd0c94636
    출처 데이터셋
    uspto-grants-2013_07
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08492560B2

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