반응 #4092
ord-d09dbf951ae649f09f2b17df1b6aceb5
반응 방정식
반응 조건
후처리
- 1온도was refluxed for 7 hours under nitrogen
- 2기타The excess phosphorus oxychloride was removed at aspirator pressure with gentle warming
- 3온도The residue was chilled in an ice-bath (with exclusion of moisture)
- 4workup.ADDITIONtreated first with 250 ml of ice-cold 2N-NaOH
- 5기타The organic phase was separated
- 6세척washed thrice with water
- 7건조dried over Na2SO4
- 8농축concentrated in vacuo to 8.5 g (98%) of an oil
- 9workup.ADDITIONcontaining 350 g of alumina
- 10세척Elution with CH2Cl2
- 11농축concentrated
- 12기타to afford
- 13기타4.6 g (53% overall yield) of product as a foam
- 14기타This was crystallized from a small volume of methanol
실험 절차
A stirred mixture of 9.14 g (0.022 mole) of N-[5-bromo-2-(2,3-dihydro-1H-indol-1-yl)phenyl]-4-methyl-1-piperazinecarboxamide of Example 3c in 250 ml of phosphorus oxychloride was refluxed for 7 hours under nitrogen then cooled to room temperature. The excess phosphorus oxychloride was removed at aspirator pressure with gentle warming. The residue was chilled in an ice-bath (with exclusion of moisture) and then treated first with 250 ml of ice-cold 2N-NaOH, then with 500 ml of dichloromethane. The mixture was stirred vigorously until all the material passed into solution. The organic phase was separated, washed thrice with water, dried over Na2SO4 and concentrated in vacuo to 8.5 g (98%) of an oil. This material was adsorbed on a tall chromatography column containing 350 g of alumina made up in CH2Cl2. Elution with CH2Cl2 brought forth fractions of virtually pure tetracycle which were combined and concentrated to afford 4.6 g (53% overall yield) of product as a foam. This was crystallized from a small volume of methanol to furnish 2.6 g of 9-bromo-6-(4-methyl-1-piperazinyl)-1,2-dihydrobenzo[b]pyrrolo[3,2,1-jk][1,4]benzodiazepine, m.p. 153°-155° C.