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Phosphorus oxychloride → 6-Fluoroimidazo[1,5-A]pyridine

HRID 245847
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HRID 245847 반응식
[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][NH:9][CH:10]=O)=[N:6][CH:7]=1.P(Cl)(Cl)(Cl)=O>C1(C)C=CC=CC=1>[F:1][C:2]1[CH:3]=[CH:4][C:5]2[N:6]([CH:10]=[N:9][CH:8]=2)[CH:7]=1
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참가 물질

4

반응물 2

HCID 24813Phosphorus oxychlorideHCID 86677902N-(5-fluoropyridin-2-ylmethyl)-formamide

생성물 1

HCID 717440036-Fluoroimidazo[1,5-A]pyridine수율 96%

시약·촉매·용매 1

HCID 1140Toluene용매

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온도
100 °C

실험 절차

In a round-bottomed flask, N-(5-fluoro-pyridin-2-ylmethyl)-formamide (612 mg, 3.97 mmol) was dissolved in toluene (16 ml) and phosphorus oxychloride (0.68 ml, 7.3 mmol) was added. The reaction mixture was stirred at 100° C. in an oil bath for 4 h then cooled to 0° C. and carefully quenched with ice. Aqueous 25% ammonium hydroxide was added until pH=˜9. The mixture was diluted with water and extracted with dichloromethane (3×). The organic layers were combined, dried over sodium sulfate, filtered and concentrated to give 517 mg (96%) of 6-fluoro-imidazo[1,5-a]pyridine as a light brown oil. 1H NMR (CDCl3, 300 MHz): δ (ppm) 8.16 (s, 1H), 7.84-7.94 (m, 1H), 7.50 (s, 1H), 7.46 (dd, J=9.8, 5.3 Hz, 1H), 6.69 (ddd, J=9.8, 7.7, 2.1 Hz, 1H).

후처리

  1. temperaturethen cooled to 0° C.
  2. customcarefully quenched with ice
  3. additionAqueous 25% ammonium hydroxide was added until pH=˜9
  4. additionThe mixture was diluted with water
  5. extractionextracted with dichloromethane (3×)
  6. dry with materialdried over sodium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated

출처 및 근거

ORD 기록
ord-c3a2821918b145de94ff4b42882b74b3
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08658646B2

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