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Sodium hydride → 1-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-5-bromopyridin-2(1H)-one

HRID 336629
ノート
印刷プレビュー

反応式

HRID 336629 の反応式
[H-].[Na+].[Br:3][C:4]1[CH:5]=[CH:6][C:7](=[O:10])[NH:8][CH:9]=1.Br[CH2:12][C:13]12[CH2:22][CH:17]3[CH2:18][CH:19]([CH2:21][CH:15]([CH2:16]3)[CH2:14]1)[CH2:20]2>CN(C)C=O>[C:13]12([CH2:12][N:8]3[CH:9]=[C:4]([Br:3])[CH:5]=[CH:6][C:7]3=[O:10])[CH2:14][CH:15]3[CH2:21][CH:19]([CH2:18][CH:17]([CH2:16]3)[CH2:22]1)[CH2:20]2
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

5

反応物 3

HCID 24758Sodium hydrideHCID 5995285-Bromo-2-hydroxypyridineHCID 14163041-(Bromomethyl)adamantane

生成物 1

HCID 866812751-(tricyclo[3.3.1.13,7]dec-1-ylmethyl)-5-bromopyridin-2(1H)-one

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
120 °C

実験手順

To an ambient suspension of NaH (185 mg, 4.63 mmol, 60% dispersion in mineral oil) in N,N-dimethylformamide (30 mL) was added 5-bromopyridin-2(1H)-one (700 mg, 4.02 mmol). The reaction mixture was stirred for 15 minutes, and 1-(bromomethyl)adamantane (968 mg 4.22 mmol) was added. The mixture was heated to 120° C. overnight, cooled to room temperature, and quenched by the addition of water and ether. The layers were separated, and the aqueous extracted with additional ether (twice). The combined organics were washed with brine, dried over Na2SO4, and filtered. Chromatography on silica gel, eluting with a gradient of 5 to 30% ethyl acetate in hexanes, provided the title compound.

後処理

  1. temperaturecooled to room temperature
  2. customquenched by the addition of water and ether
  3. customThe layers were separated
  4. extractionthe aqueous extracted with additional ether (twice)
  5. washThe combined organics were washed with brine
  6. dry with materialdried over Na2SO4
  7. filtrationfiltered
  8. washChromatography on silica gel, eluting with a gradient of 5 to 30% ethyl acetate in hexanes

出典と根拠

ORDレコード
ord-520b6d60f81244c98b4b95ecbb87bff4
出典データセット
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08889675B2

反応ノート

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