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N-[2-(t-butylamino)-5-chloro-3,6-difluoropyridin-4-yl]phthalimide → N-(2-amino-5-chloro-3,6-difluoropyridin-4-yl)phthalimide

HRID 1274723
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인쇄 미리보기

반응식

HRID 1274723 반응식
C([NH:5][C:6]1[C:11]([F:12])=[C:10]([N:13]2[C:17](=[O:18])[C:16]3=[CH:19][CH:20]=[CH:21][CH:22]=[C:15]3[C:14]2=[O:23])[C:9]([Cl:24])=[C:8]([F:25])[N:7]=1)(C)(C)C>FC(F)(F)C(O)=O>[NH2:5][C:6]1[C:11]([F:12])=[C:10]([N:13]2[C:14](=[O:23])[C:15]3=[CH:22][CH:21]=[CH:20][CH:19]=[C:16]3[C:17]2=[O:18])[C:9]([Cl:24])=[C:8]([F:25])[N:7]=1
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참가 물질

3

반응물 1

HCID 22121242N-[2-(t-butylamino)-5-chloro-3,6-difluoropyridin-4-yl]phthalimide

생성물 1

HCID 22121177N-(2-amino-5-chloro-3,6-difluoropyridin-4-yl)phthalimide

시약·촉매·용매 1

HCID 6422Trifluoroacetic acid용매

반응 조건

온도
70 °C

실험 절차

To 80 ml of trifluoroacetic acid was added all amount of the N-[2-(t-butylamino)-5-chloro-3,6-difluoropyridine-4-yl]phthalimide, and the mixture was stirred at 70° C. for 5 and half hours. The solution was concentrated under reduced pressure. The precipitate was dispersed in chloroform, and collected by filtration to obtain 19.5 g of the title compound as a colorless powder.

후처리

  1. concentrationThe solution was concentrated under reduced pressure
  2. additionThe precipitate was dispersed in chloroform
  3. filtrationcollected by filtration

출처 및 근거

ORD 기록
ord-4785d1542be64f91915dcca450376962
출처 데이터셋
uspto-grants-2000_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06156903

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