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Pyrrolidine → 2-Bromo-4-(pyrrolidin-1-yl)pyridine

HRID 537261
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HRID 537261 반응식
[Br:1][C:2]1[CH:7]=[C:6]([Br:8])[CH:5]=[CH:4][N:3]=1.[NH:9]1[CH2:13][CH2:12][CH2:11][CH2:10]1>C(O)C>[Br:1][C:2]1[CH:7]=[C:6]([N:9]2[CH2:13][CH2:12][CH2:11][CH2:10]2)[CH:5]=[CH:4][N:3]=1.[Br:8][C:6]1[CH:5]=[CH:4][N:3]=[C:2]([N:9]2[CH2:13][CH2:12][CH2:11][CH2:10]2)[CH:7]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 31268PyrrolidineHCID 8171042,4-Dibromopyridine

생성물 2

HCID 105372692-Bromo-4-(pyrrolidin-1-yl)pyridineHCID 457879184-Bromo-2-pyrrolidin-1-ylpyridine

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
70 °C

실험 절차

2,4-Dibromopyridine (1.0 g, 4.22 mmol) was dissolved in ethanol (40 mL) and pyrrolidine (1.733 ml, 21.11 mmol) was added. The reaction mixture was stirred at 70° C. for 20 hours. The reaction mixture was cooled to room temperature and the solvent was removed in vacuo to give a pale yellow solid. The crude product was purified by chromatography on silica gel (gradient: 0-80% ethyl acetate in isohexane) to afford 2-bromo-4-(pyrrolidin-1-yl)pyridine (460 mg) as a white solid, and 4-bromo-2-(pyrrolidin-1-yl)pyridine (260 mg) as a white solid. LCMS (Method F, ES-API): RT 0.79 min, m+H=227.1/229.1.

후처리

  1. temperatureThe reaction mixture was cooled to room temperature
  2. customthe solvent was removed in vacuo
  3. customto give a pale yellow solid
  4. customThe crude product was purified by chromatography on silica gel (gradient: 0-80% ethyl acetate in isohexane)

출처 및 근거

ORD 기록
ord-a364ffb255a549ce8117bb7ccf0d9b56
출처 데이터셋
uspto-grants-2014_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08859774B2

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