Hydrochloric Acid → (7,8-Difluoro-3-methyl-2,3-dihydro-1,4-benzoxazin-4-yl)-oxoacetaldehyde oxime

HRID 729423

반응식

HRID 729423 반응식
Cl[C:2](Cl)(Cl)[CH:3]([OH:5])O.[OH2:8].O.O.O.O.O.O.O.O.O.S([O-])([O-])(=O)=O.[Na+].[Na+].[F:25][C:26]1[CH:36]=[CH:35][C:29]2[NH:30][CH:31]([CH3:34])[CH2:32][O:33][C:28]=2[C:27]=1[F:37].Cl.Cl.[NH2:40]O>O.C(O)C>[F:25][C:26]1[CH:36]=[CH:35][C:29]2[N:30]([C:3](=[O:5])[CH:2]=[N:40][OH:8])[CH:31]([CH3:34])[CH2:32][O:33][C:28]=2[C:27]=1[F:37]

참가 물질

8

반응 조건

온도
77.5 °C

실험 절차

A solution of 8.27 g (50 mmol) of chloral hydrate in 125 mL of water is treated with 112.8 g (0.35 mmol) of sodium sulfate decahydrate. The mixture is stirred and treated with a solution of 7,8-difluoro-3-methyl-3,4-dihydro-2H-benz[1,4]oxazine (Chem. Pharm. Bull., 1984; 32:4907) hydrochloride prepared by dissolving 8.26 g (44.6 mmol) of the free base in 50 mmol of concentrated hydrochloric acid in 70 mL of 50% aqueous ethanol). The reaction is stirred and a solution of 9.8 g (140 mmol) of hydroxylamine hydrochloride in 50 mL of water is added. After heating at 75 to 80° C. for 3 hours, the reaction is stirred at room temperature overnight. The resulting precipitate is removed by filtration, washed with water, and the wet filter cake is dissolved in dichloromethane. The organic solution is washed with water, dried (MgSO4), decolorized with charcoal, filtered and concentrated in vacuo to give 10.5 g of the title compound, mp 188-190° C.

후처리

  1. customprepared
  2. stirringThe reaction is stirred
  3. stirringthe reaction is stirred at room temperature overnight
  4. customThe resulting precipitate is removed by filtration
  5. washwashed with water
  6. dissolutionthe wet filter cake is dissolved in dichloromethane
  7. washThe organic solution is washed with water
  8. dry with materialdried (MgSO4)
  9. filtrationfiltered
  10. concentrationconcentrated in vacuo

출처 및 근거

ORD 기록
ord-bd84b90d5ca542f285a9517cfa559188
출처 데이터셋
uspto-grants-2009_09
특허 번호
US07582627B2

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