Trifluoroacetic acid → N-[2-(3-Cyano-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazol-8-yloxy)-ethyl]-methanesulfonamide

HRID 61721노트

반응식

HRID 61721 반응식
FC(F)(F)C(O)=O.[NH2:8][CH2:9][CH2:10][O:11][C:12]1[CH:13]=[CH:14][C:15]2[C:27](=[O:28])[C:26]3[C:25]4[C:20](=[CH:21][C:22]([C:29]#[N:30])=[CH:23][CH:24]=4)[NH:19][C:18]=3[C:17]([CH3:32])([CH3:31])[C:16]=2[CH:33]=1.C(N(C(C)C)CC)(C)C.[CH3:43][S:44](Cl)(=[O:46])=[O:45]>ClCCl.O>[C:29]([C:22]1[CH:21]=[C:20]2[C:25]([C:26]3[C:27](=[O:28])[C:15]4[CH:14]=[CH:13][C:12]([O:11][CH2:10][CH2:9][NH:8][S:44]([CH3:43])(=[O:46])=[O:45])=[CH:33][C:16]=4[C:17]([CH3:31])([CH3:32])[C:18]=3[NH:19]2)=[CH:24][CH:23]=1)#[N:30]

참가 물질

7

실험 절차

Trifluoroacetic acid salt of 8-(2-amino-ethoxy)-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile (Compound A8-2, 19 mg, 0.044 mmol) was suspended in dichloromethane (0.5 mL), added with diisopropylethylamine (0.0157 mL, 2 eq.) and methanesulfonyl chloride (0.0034 mL, 1 eq.), and then stirred at room temperature for 2 hr. The reaction solution was added to water, and then extracted with dichloromethane. After washing with saturated brine, the organic layer was dried over sodium sulfate. The drying agent was removed by filtration and the residues obtained after concentration under reduced pressure were separated by silica gel preparative TLC (ethyl acetate 100%) to obtain the target compound (5.5 mg, 29%).

후처리

  1. extractionextracted with dichloromethane
  2. washAfter washing with saturated brine
  3. dry with materialthe organic layer was dried over sodium sulfate
  4. customThe drying agent was removed by filtration
  5. customthe residues obtained
  6. concentrationafter concentration under reduced pressure
  7. customwere separated by silica gel preparative TLC (ethyl acetate 100%)

출처 및 근거

ORD 기록
ord-506c277519da482291685818c6d45abd
출처 데이터셋
uspto-grants-2016_09
특허 번호
US09440922B2

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