Sodium hydride → HCID 66919002, 화합물
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[CH:1]1([NH:4][C:5]([C:7]2[CH:8]=[CH:9][C:10]([CH3:26])=[C:11]([NH:13][C:14](=[O:25])[C:15]3[CH:20]=[C:19](F)[CH:18]=[CH:17][C:16]=3[N+:22]([O-:24])=[O:23])[CH:12]=2)=[O:6])[CH2:3][CH2:2]1.C(OC([N:34]1[CH2:38][CH2:37][CH2:36][C@H:35]1[CH2:39][OH:40])=O)(C)(C)C.[H-].[Na+].[Cl-:43].[NH4+]>CN(C=O)C>[ClH:43].[CH:1]1([NH:4][C:5]([C:7]2[CH:8]=[CH:9][C:10]([CH3:26])=[C:11]([NH:13][C:14](=[O:25])[C:15]3[CH:20]=[C:19]([O:40][CH2:39][C@@H:35]4[CH2:36][CH2:37][CH2:38][NH:34]4)[CH:18]=[CH:17][C:16]=3[N+:22]([O-:24])=[O:23])[CH:12]=2)=[O:6])[CH2:3][CH2:2]1참가 물질
실험 절차
To a solution of N-{5-[(cyclopropylamino)carbonyl]-2-methylphenyl}-5-fluoro-2-nitrobenzamide (3.0 g) and (S)-(−)-1-(tert-butoxycarbonyl)-2-pyrrolidinemethanol (2.54 g) in DMF (45 ml) was added sodium hydride (1.34 g of a 60% dispersion in oil) portion-wise (ice bath cooling). The reaction was stirred for 24 hours at room temperature under an atmosphere of argon. The reaction mixture was then poured into a saturated aqueous ammonium chloride solution (200 ml) and the resulting precipitate was collected by filtration, dissolved in methanol (10 ml) and 4N HCl in dioxane (5 ml) added. The reaction mixture was stirred at room temperature for 16 hours, concentrated and re-precipitated from methanol/ethyl acetate to yield N-{5-[(cyclopropylamino)carbonyl]-2-methylphenyl}-2-nitro-5-[(2S)-pyrrolidin-2-ylmethoxy]benzamide hydrochloride salt (2.25 g) as a yellow solid which was used without further purification; Mass Spectrum: M+H+ 439.
후처리
- temperatureportion-wise (ice bath cooling)
- filtrationthe resulting precipitate was collected by filtration
- dissolutiondissolved in methanol (10 ml)
- addition4N HCl in dioxane (5 ml) added
- stirringThe reaction mixture was stirred at room temperature for 16 hours
- concentrationconcentrated
- customre-precipitated from methanol/ethyl acetate
출처 및 근거
- ORD 기록
- ord-acedb559e6834aa4a102c8e097492030
- 출처 데이터셋
- uspto-grants-2010_07
- 특허 번호
- US07750154B2
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