Isopropylamine → 6-{[2-(3-chloro-pyridin-2-yl)-5-trifluoromethyl-2H-pyrazole-3-carbonyl]-amino}-1H-indole-7-carboxylic acid isopropylamide

HRID 245606ノート

反応式

HRID 245606 の反応式
[Cl:1][C:2]1[C:3]([N:8]2[C:12]([C:13]3[O:22][C:21](=[O:23])[C:20]4[C:15](=[CH:16][CH:17]=[C:18]5[CH:26]=[CH:25][NH:24][C:19]5=4)[N:14]=3)=[CH:11][C:10]([C:27]([F:30])([F:29])[F:28])=[N:9]2)=[N:4][CH:5]=[CH:6][CH:7]=1.[CH:31]([NH2:34])([CH3:33])[CH3:32]>O1CCCC1>[CH:31]([NH:34][C:21]([C:20]1[C:15]([NH:14][C:13]([C:12]2[N:8]([C:3]3[C:2]([Cl:1])=[CH:7][CH:6]=[CH:5][N:4]=3)[N:9]=[C:10]([C:27]([F:29])([F:28])[F:30])[CH:11]=2)=[O:22])=[CH:16][CH:17]=[C:18]2[C:19]=1[NH:24][CH:25]=[CH:26]2)=[O:23])([CH3:33])[CH3:32]

参加物

4

実験手順

To a solution of 110 mg (0.25 mmol) of the crude 7-[2-(3-chloro-pyridin-2-yl)-5-trifluoromethyl-2H-pyrazol-3-yl]-1H-8-oxa-1,6-diaza-cyclopenta[a]naphthalen-9-one in 2.5 mL of anhydrous tetrahydrofuran, under Argon, is added 0.07 mL (0.77 mmol) of isopropylamine. The reaction is stirred during 5 hours at ambient temperature and then quenched with an aqueous saturated solution of ammonium chloride. The product is extracted twice with ethyl acetate and the combined organic phases are dried on Na2SO4, filtrated and the solvent is evaporated. After purification by flash chromatography on silica gel with hexanes and ethyl acetate as eluents and a preparative thin layer chromatography, 18.5 mg (0.04 mmol, 16%) of a white solid are obtained; LC/MS:513/515 (M+Na)+, m.p.: 240-242° C.

後処理

  1. customquenched with an aqueous saturated solution of ammonium chloride
  2. extractionThe product is extracted twice with ethyl acetate
  3. customthe combined organic phases are dried on Na2SO4
  4. filtrationfiltrated
  5. customthe solvent is evaporated
  6. customAfter purification by flash chromatography on silica gel with hexanes and ethyl acetate as eluents

出典と根拠

ORDレコード
ord-2042812cf56f46dab18f4e8b1865964b
出典データセット
uspto-grants-2014_02
特許番号
US08658801B2

反応ノート

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