Triethylamine → N-[(1R,2S)-1-[1-(4-fluorophenyl)indazol-5-yl]oxy-1-(4-methylsulfanylphenyl)propan-2-yl]-2-methoxy-acetamide

HRID 13016

반응식

HRID 13016 반응식
[CH3:1][O:2][CH2:3][C:4](Cl)=[O:5].Cl.[F:8][C:9]1[CH:14]=[CH:13][C:12]([N:15]2[C:23]3[C:18](=[CH:19][C:20]([O:24][C@H:25]([C:29]4[CH:34]=[CH:33][C:32]([S:35][CH3:36])=[CH:31][CH:30]=4)[C@@H:26]([NH2:28])[CH3:27])=[CH:21][CH:22]=3)[CH:17]=[N:16]2)=[CH:11][CH:10]=1.C(N(CC)CC)C>C1COCC1>[F:8][C:9]1[CH:14]=[CH:13][C:12]([N:15]2[C:23]3[C:18](=[CH:19][C:20]([O:24][C@H:25]([C:29]4[CH:30]=[CH:31][C:32]([S:35][CH3:36])=[CH:33][CH:34]=4)[C@@H:26]([NH:28][C:4](=[O:5])[CH2:3][O:2][CH3:1])[CH3:27])=[CH:21][CH:22]=3)[CH:17]=[N:16]2)=[CH:11][CH:10]=1

참가 물질

5

실험 절차

Methoxyacetyl chloride (10 μL, 0.11 mmol) was added to a suspension of (1R,2S)-1-{[1-(4-fluorophenyl)-1H-indazol-5-yl]oxy}-1-[4-(methylthio)phenyl]propan-2-amine hydrochloride (40 mg, 0.09 mmol) and triethylamine (42 μL, 0.3 mmol) in THF (1 mL). The reaction was stirred at r.t. for 30 min and then quenched by adding water, the mixture was diluted with a small volume of MeCN so that a solution was obtained. This crude mixture was purified by semi-preparative HPLC using a Kromasil® C18 250×20 mm, 5 μm column. Flow 10 mL/min, 20 min gradient of 20%-90% MeCN in water followed by isocratic final concentration until product had eluted. UV=254 nm was used for detection. Fractions with product was combined and lyophilized to afford the title compound as a colourless solid. Yield 30 mg (69%).

후처리

  1. customquenched
  2. additionby adding water
  3. additionthe mixture was diluted with a small volume of MeCN so that a solution
  4. customwas obtained
  5. customThis crude mixture was purified by semi-preparative HPLC
  6. customFlow 10 mL/min, 20 min gradient of 20%-90% MeCN in water
  7. concentrationconcentration until product
  8. washhad eluted

출처 및 근거

ORD 기록
ord-e5c732e75a6f47b9bb790ed140987727
출처 데이터셋
uspto-grants-2010_06
특허 번호
US07728030B2

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