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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Water → 2-(7-Chloro-4-quinolinylamino)-5-fluoro-benzoic acid

HRID 224587
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인쇄 미리보기

반응식

HRID 224587 반응식
[Cl:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6]([NH:12][C:13]3[CH:22]=[CH:21][C:20]([F:23])=[CH:19][C:14]=3[C:15]([O:17]C)=[O:16])=[CH:7][CH:8]=[N:9]2)=[CH:4][CH:3]=1.[OH-].[Na+].O>CO>[Cl:1][C:2]1[CH:11]=[C:10]2[C:5]([C:6]([NH:12][C:13]3[CH:22]=[CH:21][C:20]([F:23])=[CH:19][C:14]=3[C:15]([OH:17])=[O:16])=[CH:7][CH:8]=[N:9]2)=[CH:4][CH:3]=1
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참가 물질

5

반응물 3

HCID 962WaterHCID 14798Sodium HydroxideHCID 23331682Methyl 2-(7-chloro-4-quinolinylamino)-5-fluoro-benzoate

생성물 1

HCID 233316862-(7-Chloro-4-quinolinylamino)-5-fluoro-benzoic acid수율 99.5%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of 1.8 g of the ester of Example 1, 25 ml of N sodium hydroxide solution, 25 ml of water and 100 ml of methanol was heated at 70°-75° C. for 90 minutes and the methanol was then evaporated. 100 ml of water and 10 ml of dimethylformamide were added to the mixture which was then heated to reflux. 4 ml of acetic acid were added thereto and the mixture was held in an ice bath for an hour and was then vacuum filtered. The recovered crystals were washed with water and dried to obtain 1.715 g of 2-(7-chloro-4-quinolinylamino)-5-fluoro-benzoic acid melting at 341°-342° C.

후처리

  1. customthe methanol was then evaporated
  2. addition100 ml of water and 10 ml of dimethylformamide were added to the mixture which
  3. temperaturewas then heated to reflux
  4. addition4 ml of acetic acid were added
  5. waitthe mixture was held in an ice bath for an hour
  6. filtrationvacuum filtered
  7. washThe recovered crystals were washed with water
  8. customdried

출처 및 근거

ORD 기록
ord-688202f6158442129ddb04a5b7e6061c
출처 데이터셋
uspto-grants-1980_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04233305

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