Dimethylformamide → 5,6,7,8-Tetrahydro-2-(2-methoxy-4-methylsulfonylphenyl)imidazo[1,2-a]pyrazine dihydrochloride

HRID 483083노트

반응식

HRID 483083 반응식
Br.[Cl:2][C:3]1[C:4]2[N:5]([CH:9]=[C:10]([C:12]3[CH:17]=[CH:16][C:15]([S:18]([CH3:21])(=[O:20])=[O:19])=[CH:14][C:13]=3[O:22][CH3:23])[N:11]=2)[CH:6]=[CH:7][N:8]=1.CN(C)C=O>[Pd].C(N(CC)CC)C>[ClH:2].[ClH:2].[CH3:23][O:22][C:13]1[CH:14]=[C:15]([S:18]([CH3:21])(=[O:20])=[O:19])[CH:16]=[CH:17][C:12]=1[C:10]1[N:11]=[C:4]2[CH2:3][NH:8][CH2:7][CH2:6][N:5]2[CH:9]=1

참가 물질

5

실험 절차

A suspension of 4.5 g. of 8-chloro-2-(2-methoxy-4-methylsulfonylphenyl)imidazo[1,2-a]pyrazine hydrobromide in 190 ml. of dimethylformamide was treated with 3.4 g. of triethylamine and 1 g. of 5% palladium-on-carbon. This mixture was hydrogenated at room temperature at 60 psi for about 75 minutes. The catalyst was removed by filtration and the solvent was removed in vacuo. During the course of solvent removal a precipitate occurred which was removed by filtration. The precipitate was triturated with chloroform and the residue was suspended in methanolic hydrogen chloride. After stirring for a period of time, the methanol was removed by evaporation and the resulting solid was collected with acetone by filtration affording 2.1 g. of the desired title product, M+ =307.

후처리

  1. additionA suspension of 4.5 g
  2. customThe catalyst was removed by filtration
  3. customthe solvent was removed in vacuo
  4. customDuring the course of solvent removal a precipitate
  5. customwas removed by filtration
  6. customThe precipitate was triturated with chloroform
  7. customthe methanol was removed by evaporation
  8. filtrationthe resulting solid was collected with acetone by filtration
  9. customaffording 2.1 g

출처 및 근거

ORD 기록
ord-85b58babf2df4945a1a002652808ef7c
출처 데이터셋
uspto-grants-1986_03
특허 번호
US04578387

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