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Water → 5-Bromo-2-(2-pyrrolidin-1-yl-ethoxy)-pyrimidine

HRID 1916569
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HRID 1916569 반응식
[H-].[Na+].[OH:3][CH2:4][CH2:5][N:6]1[CH2:10][CH2:9][CH2:8][CH2:7]1.[Br:11][C:12]1[CH:13]=[N:14][C:15](Cl)=[N:16][CH:17]=1.O>C1COCC1>[Br:11][C:12]1[CH:13]=[N:14][C:15]([O:3][CH2:4][CH2:5][N:6]2[CH2:10][CH2:9][CH2:8][CH2:7]2)=[N:16][CH:17]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 962WaterHCID 24758Sodium hydrideHCID 762881-PyrrolidineethanolHCID 6066655-Bromo-2-chloropyrimidine

생성물 1

HCID 638675465-Bromo-2-(2-pyrrolidin-1-yl-ethoxy)-pyrimidine

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

50 mg (1.15 mmol, 60%) NaH are added to a solution of 0.17 mL (1.38 mmol) N-(2-hydroxyethyl)pyrrolidine in 10 mL THF at RT. The reaction solution is stirred for 15 min at RT and then 200 mg (1.03 mmol) 5-bromo-2-chloropyrimidine are added. The solution is stirred for 16 h at RT. 10 mL water are added and the aqueous phase is extracted with 20 mL EtOAc. The organic phase is dried over Na2SO4 and the solvent is eliminated i.vac. Further purification is carried out by column chromatography on silica gel (DCM/MeOH/NH3 9:1:0.1).

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후처리

  1. stirringThe solution is stirred for 16 h at RT
  2. extractionthe aqueous phase is extracted with 20 mL EtOAc
  3. dry with materialThe organic phase is dried over Na2SO4
  4. customFurther purification

출처 및 근거

ORD 기록
ord-5e05170c2e294bd9b34ead06234b3776
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08618132B2

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