2-Aminopyridine → HCID 18008032, 화합물

HRID 988221

반응식

HRID 988221 반응식
[NH2:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][N:3]=1.Br[CH:9]([CH2:15][C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1)[C:10](OCC)=[O:11].[Na].[F:23][C:24]1[CH:31]=[CH:30][C:27]([CH2:28]Br)=[CH:26][CH:25]=1>CCOCC.C(O)C>[CH2:15]([C:9]1([CH2:28][C:27]2[CH:30]=[CH:31][C:24]([F:23])=[CH:25][CH:26]=2)[N:3]2[CH:4]=[CH:5][CH:6]=[CH:7][C:2]2=[N:1][C:10]1=[O:11])[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1

참가 물질

7

반응물 4

HCID 104392-AminopyridineHCID 680214-Fluorobenzyl bromideHCID 4737529Ethyl 2-bromo-3-phenylpropanoateHCID 5360545Sodium

생성물 1

HCID 18008032HCID 18008032, 화합물수율 1%

시약·촉매·용매 2

HCID 702Ethanol용매HCID 3283Diethyl Ether용매

실험 절차

630 mg (6.7 mmol) of 2-aminopyridine and 1.72 g (6.7 mmol) of ethyl 2-bromo-3-phenylpropionate were refluxed under heating in 50 ml of ether for 12 hours. The reaction mixture was allowed to cool to room temperature and ether was removed by decantation. The residue was added with and dissolved in 30 ml of absolute ethanol, which was added to a solution of 150 mg (6.5 mmol) of sodium in 10 ml of absolute ethanol and stirred at room temperature for one hour. Then, 0.8 ml (6.5 mmol) of 4-fluorobenzylbromide was added and stirred for overnight. The reaction mixture was added to ice water and extracted with methylene chloride. Then, the solvent was removed under reduced pressure and the residue was purified with silica gel column chromatography, thus obtaining 22 mg (yield: 1%) of the titled compound.

후처리

  1. customether was removed by decantation
  2. additionThe residue was added with and
  3. dissolutiondissolved in 30 ml of absolute ethanol
  4. stirringstirred for overnight
  5. extractionextracted with methylene chloride
  6. customThen, the solvent was removed under reduced pressure
  7. customthe residue was purified with silica gel column chromatography

출처 및 근거

ORD 기록
ord-341b7fbd82a845f494565c5adfd8bd14
출처 데이터셋
uspto-grants-2003_10
특허 번호
US06635652B1

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