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

HRID 336629
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HRID 336629 반응식
[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
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참가 물질

5

반응물 3

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

생성물 1

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

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
120 °C

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-520b6d60f81244c98b4b95ecbb87bff4
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08889675B2

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