Methanol → 7-(hydroxymethyl)-4-methyl-3,4-dihydropyrido[2,3-b]pyrazin-2(1H)-one

HRID 69643

반응식

HRID 69643 반응식
[CH3:1][N:2]1[CH2:7][C:6](=[O:8])[NH:5][C:4]2[CH:9]=[C:10]([C:13](OC)=[O:14])[CH:11]=[N:12][C:3]1=2.[H-].[Na+].[H-].[Al+3].[Li+].[H-].[H-].[H-].CO>O1CCCC1.O.C(OCC)(=O)C>[OH:14][CH2:13][C:10]1[CH:11]=[N:12][C:3]2[N:2]([CH3:1])[CH2:7][C:6](=[O:8])[NH:5][C:4]=2[CH:9]=1

참가 물질

8

반응 조건

온도
-45 °C

실험 절차

Methyl 4-methyl-2-oxo-1,2,3,4-tetrahydropyrido[2,3-b]pyrazine-7-carboxylate (500 mg, 2.25 mmol) was taken up in tetrahydrofuran (25 mL) in an inert environment. To the stirred suspension at room temperature was added NaH (60% dispersion in mineral oil, 136 mg, 3.40 mmol) and stirred 30 min. The reaction was then cooled to −45° C. and lithium aluminum hydride (2M in THF, 3.3 mL, 6.6 mmol) was added. The reaction was stirred at a temperature between −20 and −10° C. for 1 h. The reaction was then cooled back to −60° C. and MeOH (1 mL) followed by water (1 mL) was added. The reaction was allowed to stir at ambient temperature for 2 h and then poured into ethyl acetate (300 mL) and water (200 mL). The biphasic mixture was stirred vigorously and then filtered through a medium frit. The layers were separated and the aqueous phase was extracted with ethyl acetate (3×100 mL). The organic layers were combined, washed with brine (100 mL), dried with sodium sulfate and concentrated to yield the title compound (415 mg, 95%) as a white solid. [M+H] calc'd for C9H11N3O2, 194; found, 194.

후처리

  1. stirringThe reaction was stirred at a temperature between −20 and −10° C. for 1 h
  2. temperatureThe reaction was then cooled back to −60° C.
  3. additionwas added
  4. stirringto stir at ambient temperature for 2 h
  5. stirringThe biphasic mixture was stirred vigorously
  6. filtrationfiltered through a medium frit
  7. customThe layers were separated
  8. extractionthe aqueous phase was extracted with ethyl acetate (3×100 mL)
  9. washwashed with brine (100 mL)
  10. dry with materialdried with sodium sulfate
  11. concentrationconcentrated

출처 및 근거

ORD 기록
ord-9360788446664a4db6d32675b7518459
출처 데이터셋
uspto-grants-2014_09
특허 번호
US08822470B2

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