Hydrochloric Acid → Methyl 4-butyl-8-cyano-3,4-dihydro-2H-1,4-benzoxazine-6-carboxylate

HRID 14194

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HRID 14194 반응식
Br[C:2]1[C:11]2[O:10][CH2:9][CH2:8][N:7]([CH2:12][CH2:13][CH2:14][CH3:15])[C:6]=2[CH:5]=[C:4]([C:16]([O:18][CH3:19])=[O:17])[CH:3]=1.[Cu](C#N)[C:21]#[N:22].Cl>CN1C(=O)CCC1>[CH2:12]([N:7]1[C:6]2[CH:5]=[C:4]([C:16]([O:18][CH3:19])=[O:17])[CH:3]=[C:2]([C:21]#[N:22])[C:11]=2[O:10][CH2:9][CH2:8]1)[CH2:13][CH2:14][CH3:15]

참가 물질

5

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온도
175 °C

실험 절차

To a flask containing methyl 8-bromo-4-butyl-3,4-dihydro-2H-1,4-benzoxazine-6-carboxylate (0.33 g) was added NMP (7 mL), followed by copper cyanide (0.18 g). The mixture was then heated to 175° C. and stirred overnight. The resulting mixture was cooled to room temperature and poured into 1 N hydrochloric acid. The acidic aqueous layer was extracted with ethyl acetate, washed with 1 N hydrochloric acid (15 mL), saturated sodium bicarbonate (15 mL), and brine, dried (magnesium sulfate), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica, 1:9 ethyl acetate/hexanes) provided 184 mg of the title compound: 1H NMR (300 MHz, CDCl3) δ 7.55, 7.43, 4.41, 3.89, 3.39, 3.31, 1.58, 1.40, 0.97.

후처리

  1. temperatureThe resulting mixture was cooled to room temperature
  2. extractionThe acidic aqueous layer was extracted with ethyl acetate
  3. washwashed with 1 N hydrochloric acid (15 mL), saturated sodium bicarbonate (15 mL), and brine
  4. dry with materialdried (magnesium sulfate)
  5. filtrationfiltered
  6. concentrationconcentrated under reduced pressure
  7. customPurification by flash column chromatography (silica, 1:9 ethyl acetate/hexanes)

출처 및 근거

ORD 기록
ord-c734aefb23a24984b9ddb1e684b7fdcb
출처 데이터셋
uspto-grants-2010_06
특허 번호
US07727997B2

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