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Sodium hydride → 1-(4-Chloro-1-phenyl-1H-pyrazolo[3,4-b]pyridin-5-yl)-2,2,2-trifluoro-1-(1H-pyrrolo[2,3-b]pyridin-3-yl)ethanol

HRID 244395
ノート
印刷プレビュー

反応式

HRID 244395 の反応式
[F:1][C:2]([F:15])([F:14])[C:3]([C:5]1[C:13]2[C:8](=[N:9][CH:10]=[CH:11][CH:12]=2)[NH:7][CH:6]=1)=[O:4].[H-].[Na+].Br[C:19]1[C:20]([Cl:34])=[C:21]2[CH:27]=[N:26][N:25]([C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=3)[C:22]2=[N:23][CH:24]=1.[Li]CCCC.[Na]>C1COCC1.[Cl-].[NH4+]>[Cl:34][C:20]1[C:19]([C:3]([C:5]2[C:13]3[C:8](=[N:9][CH:10]=[CH:11][CH:12]=3)[NH:7][CH:6]=2)([OH:4])[C:2]([F:1])([F:14])[F:15])=[CH:24][N:23]=[C:22]2[N:25]([C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][CH:29]=3)[N:26]=[CH:27][C:21]=12
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

8

反応物 5

HCID 24758Sodium hydrideHCID 5360545SodiumHCID 57078082,2,2-trifluoro-1-(1H-pyrrolo[2,3-b]pyridin-3-yl)ethanone2 回HCID 684797205-bromo-4-chloro-1-phenyl-1H-pyrazolo[3,4-b]pyridineHCID 178418339Butyllithium

生成物 1

HCID 24958727
1-(4-Chloro-1-phenyl-1H-pyrazolo[3,4-b]pyridin-5-yl)-2,2,2-trifluoro-1-(1H-pyrrolo[2,3-b]pyridin-3-yl)ethanol
収率 46%

試薬・触媒・溶媒 2

HCID 8028Tetrahydrofuran溶媒2 回HCID 25517Ammonium Chloride溶媒

反応条件

温度
-78 °C

実験手順

To a chilled (ice-bath) solution of 369 mg (1.72 mmol) of 2,2,2-trifluoro-1-(1H-pyrrolo[2,3-b]pyridin-3-yl)ethanone in 10 mL of THF was added 70 mg (1.75 mmol) of 60% sodium hydride in mineral oil and the mixture was then chilled to −78° C. In another flask, to a chilled (−78° C.) solution of 508 mg (1.65 mmol) of 5-bromo-4-chloro-1-phenyl-1H-pyrazolo[3,4-b]pyridine (prepared according to the procedures in Misra, Bioorg. Med. Chem. Lett. 2003, 13, 2405, and Nakai in Chem. Pharm. Bull. 2004, 52, 1098) in 10 mL of anhydrous THF was added 670 μL (1.68 mmol) of a 2.5 M solution of n-BuLi in hexanes. The mixture stirred for 5 minutes and was then added to the sodium salt of 2,2,2-trifluoro-1-(1H-pyrrolo[2,3-b]pyridin-3-yl)ethanone. The reaction was monitored by TLC [ethyl acetate-hexanes (6:4)] indicating a new more polar product than both starting materials. After 1 hour, the mixture was diluted with 30 mL of saturated aqueous ammonium chloride and extracted with three 30 mL portions of ethyl acetate. The combined organic layers were washed with three 30 mL portions of brine, dried over magnesium sulfate, filtered, and concentrated in vacuo. The crude residue was chromatographed on silica gel using dichloromethane to load the sample and then eluting with ethyl acetate-hexanes (10-50% gradient) to afford 337 mg (44%) of title compound. Trituration with ether afforded 85 mg of the title compound as a white solid. MS m/z 444.38 (MH+).

後処理

  1. customprepared
  2. waitAfter 1 hour
  3. extractionextracted with three 30 mL portions of ethyl acetate
  4. washThe combined organic layers were washed with three 30 mL portions of brine
  5. dry with materialdried over magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated in vacuo
  8. customThe crude residue was chromatographed on silica gel
  9. washeluting with ethyl acetate-hexanes (10-50% gradient)

出典と根拠

ORDレコード
ord-0b42e52c0dde4f62af5e244619827c6c
出典データセット
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08658637B2

反応ノート

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