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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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7-Benzyloxy-4-(4-bromo-2,6-difluoroanilino)-6-methoxyquinazoline → 4-(4-Bromo-2,6-difluoroanilino)-7-hydroxy-6-methoxyquinazoline

HRID 238114
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HRID 238114 반응식
C([O:8][C:9]1[CH:18]=[C:17]2[C:12]([C:13]([NH:19][C:20]3[C:25]([F:26])=[CH:24][C:23]([Br:27])=[CH:22][C:21]=3[F:28])=[N:14][CH:15]=[N:16]2)=[CH:11][C:10]=1[O:29][CH3:30])C1C=CC=CC=1>C(O)(C(F)(F)F)=O>[Br:27][C:23]1[CH:22]=[C:21]([F:28])[C:20]([NH:19][C:13]2[C:12]3[C:17](=[CH:18][C:9]([OH:8])=[C:10]([O:29][CH3:30])[CH:11]=3)[N:16]=[CH:15][N:14]=2)=[C:25]([F:26])[CH:24]=1
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참가 물질

3

반응물 1

HCID 107906057-Benzyloxy-4-(4-bromo-2,6-difluoroanilino)-6-methoxyquinazoline

생성물 1

HCID 1354935444-(4-Bromo-2,6-difluoroanilino)-7-hydroxy-6-methoxyquinazoline수율 98%

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

실험 절차

Using an analogous procedure to that described for the synthesis of the starting material in Example 8, 7-benzyloxy-4-(4-bromo-2,6-difluoroanilino)-6-methoxyquinazoline (1.9 g, 4.02 mmol) was reacted with TFA (20 ml) to give 4-(4-bromo-2,6-difluoroanilino)-7-hydroxy-6-methoxyquinazoline (1.5 g, 98%).

출처 및 근거

ORD 기록
ord-af756cdcaeec46bf8af0d22612aa3663
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08642608B2

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