홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

Trifluoroacetic acid → 3-(3-(cyclopropanecarboxamido)-1H-indazol-6-ylamino)-4-methyl-N-(3-(trifluoro-methyl)phenyl)benzamide

HRID 876896
노트
인쇄 미리보기

반응식

HRID 876896 반응식
[CH:1]1([C:4]([NH:6][C:7]2[C:15]3[C:10](=[CH:11][C:12]([NH:16][C:17]4[CH:18]=[C:19]([CH:33]=[CH:34][C:35]=4[CH3:36])[C:20]([NH:22][C:23]4[CH:28]=[CH:27][CH:26]=[C:25]([C:29]([F:32])([F:31])[F:30])[CH:24]=4)=[O:21])=[CH:13][CH:14]=3)[N:9](COCC[Si](C)(C)C)[N:8]=2)=[O:5])[CH2:3][CH2:2]1.[C:45]([OH:51])([C:47]([F:50])([F:49])[F:48])=[O:46]>C(Cl)Cl>[C:45]([OH:51])([C:47]([F:50])([F:49])[F:48])=[O:46].[CH:1]1([C:4]([NH:6][C:7]2[C:15]3[C:10](=[CH:11][C:12]([NH:16][C:17]4[CH:18]=[C:19]([CH:33]=[CH:34][C:35]=4[CH3:36])[C:20]([NH:22][C:23]4[CH:28]=[CH:27][CH:26]=[C:25]([C:29]([F:31])([F:30])[F:32])[CH:24]=4)=[O:21])=[CH:13][CH:14]=3)[NH:9][N:8]=2)=[O:5])[CH2:3][CH2:2]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 6422Trifluoroacetic acidHCID 674006613-(3-(cyclopropanecarboxamido)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-indazol-6-ylamino)-4-methyl-N-(3-(trifluoromethyl)phenyl)benzamide

생성물 2

HCID 6422Trifluoroacetic acidHCID 682341303-(3-(cyclopropanecarboxamido)-1H-indazol-6-ylamino)-4-methyl-N-(3-(trifluoro-methyl)phenyl)benzamide수율 66%

시약·촉매·용매 1

HCID 6344
Dichloromethane
용매

실험 절차

To a solution of 3-(3-(cyclopropanecarboxamido)-1-((2-(trimethylsilyl)ethoxy)methyl)-1H-indazol-6-ylamino)-4-methyl-N-(3-(trifluoromethyl)phenyl)benzamide (25 mg) in CH2Cl2 (1 mL) was added TFA (0.25 mL) at room temperature. The reaction mixture was stirred for 2 hours and the organic solvent was concentrated under reduced pressure. To a solution of the resulting mixture in THF (0.5 mL) and MeOH (0.5 mL) was added LiOH aqueous solution (1.0 M, 1.0 mL). The resulting mixture was stirred for another 2 hours at room temperature. The organic solvent was removed under reduced pressure and the aqueous layer was extracted with ethyl acetate. The organic extracts were washed with brine, dried over MgSO4 and concentrated under reduced pressure. The crude product was purified by Prep HPLC and acetonitrile was removed under reduced pressure. The remained water was freeze-dried to afford TFA salt of title compound (16 mg, 66%), MS (ESI) m/z 494 (M+H)+.

후처리

  1. concentrationthe organic solvent was concentrated under reduced pressure
  2. additionTo a solution of the resulting mixture in THF (0.5 mL) and MeOH (0.5 mL) was added LiOH aqueous solution (1.0 M, 1.0 mL)
  3. stirringThe resulting mixture was stirred for another 2 hours at room temperature
  4. customThe organic solvent was removed under reduced pressure
  5. extractionthe aqueous layer was extracted with ethyl acetate
  6. washThe organic extracts were washed with brine
  7. dry with materialdried over MgSO4
  8. concentrationconcentrated under reduced pressure
  9. customThe crude product was purified by Prep HPLC and acetonitrile
  10. customwas removed under reduced pressure
  11. dry with materialThe remained water was freeze-dried

출처 및 근거

ORD 기록
ord-9baaf77a3f124a35afddd07456819914
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08987275B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트