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

HRID 245841
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HRID 245841 반응식
P(Cl)(Cl)(Cl)=O.[CH3:6][C:7]1[CH:8]=[CH:9][C:10]([CH2:13][NH:14][CH:15]=O)=[N:11][CH:12]=1>C1(C)C=CC=CC=1>[CH3:6][C:7]1[CH:8]=[CH:9][C:10]2[N:11]([CH:15]=[N:14][CH:13]=2)[CH:12]=1
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참가 물질

4

반응물 2

HCID 24813Phosphorus oxychlorideHCID 86677901N-(5-methyl-pyridin-2-ylmethyl)-formamide

생성물 1

HCID 594583226-Methylimidazo[1,5-A]pyridine수율 41%

시약·촉매·용매 1

HCID 1140Toluene용매

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온도
100 °C

실험 절차

In a round-bottomed flask, N-(5-methyl-pyridin-2-ylmethyl)-formamide (crude from step 2) was dissolved in toluene (30 ml) and phosphorus oxychloride (1.2 ml, 12.9 mmol) was added. The reaction mixture was stirred at 100° C. in an oil bath overnight 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 (2×). The organic layers were combined, dried over sodium sulfate, filtered and concentrated. The residue was absorbed on silica gel and chromatographed with EtOAc/hexanes (gradient 0-80% EtOAc) to give 386 mg (41%, 3 steps) of 6-methyl-imidazo[1,5-a]pyridine as a light brown solid. 1H NMR (CDCl3, 300 MHz): δ (ppm) 8.09 (s, 1H), 7.74 (s, 1H), 7.32-7.43 (m, 2H), 6.60 (dd, J=9.4, 1.1 Hz, 1H), 2.25 (d, J=1.1 Hz, 3H).

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 (2×)
  6. dry with materialdried over sodium sulfate
  7. filtrationfiltered
  8. concentrationconcentrated
  9. customThe residue was absorbed on silica gel
  10. customchromatographed with EtOAc/hexanes (gradient 0-80% EtOAc)

출처 및 근거

ORD 기록
ord-a76a6aa1332c4b75aec1b29302a5f204
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08658646B2

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