Sodium Bicarbonate → 8-(4-Methyl-piperazin-1-yl)-3phenylsulfonylquinoline

HRID 271137

반응식

HRID 271137 반응식
I[C:2]1[CH:3]=[N:4][C:5]2[C:10]([CH:11]=1)=[CH:9][CH:8]=[CH:7][C:6]=2[N:12]1[CH2:17][CH2:16][N:15]([CH3:18])[CH2:14][CH2:13]1.BrC1C=NC2C(C=1)=CC=CC=2N1CCN(C)CC1.[Na+].[C:38]1([S:44]([O-:46])=[O:45])[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=1.C(=O)([O-])O.[Na+]>CN(C)C=O.[Cu]I.CO.ClCCl>[CH3:18][N:15]1[CH2:16][CH2:17][N:12]([C:6]2[CH:7]=[CH:8][CH:9]=[C:10]3[C:5]=2[N:4]=[CH:3][C:2]([S:44]([C:38]2[CH:43]=[CH:42][CH:41]=[CH:40][CH:39]=2)(=[O:46])=[O:45])=[CH:11]3)[CH2:13][CH2:14]1

참가 물질

9

반응물 4

HCID 516892Sodium BicarbonateHCID 2723840Benzenesulfinic acid, sodium saltHCID 673136243-Bromo-8-(4-methyl-piperazin-1-yl)-quinolineHCID 673137463-Iodo-8-(4-methyl-piperazin-1-yl)-quinoline

생성물 1

HCID 99291628-(4-Methyl-piperazin-1-yl)-3phenylsulfonylquinoline수율 7%

시약·촉매·용매 4

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)촉매HCID 887Methanol용매HCID 6228Dimethylformamide용매HCID 6344Dichloromethane용매

반응 조건

온도
120 °C

실험 절차

A 4:1 mixture of 3-iodo-8-(4-methyl-piperazin-1-yl)-quinoline (D2) and 3-bromo-8-(4-methyl-piperazin-1-yl)-quinoline (D1) (1.5 g), phenylsulfinic acid sodium salt, dihydrate (2.52 g, 12.6 mmol) and copper (I) iodide (2.4 g, 12.6 mmol) in N,N-dimethylformamide (25 ml) was stirred in an oil bath at 120° C. for 40 h under argon. To the reaction mixture, cooled to ambient temperature, was added 5% sodium hydrogen carbonate solution (100 ml) and dichloromethane (100 ml) with vigorous shaking. The insoluble material was filtered, washed with dichloromethane (3×20 ml) and discarded. The filtrate and washings were transferred to a separating funnel and the layers separated. The aqueous layer was extracted with dichloromethane (100 ml) and the combined organic extracts were washed with water (100 ml), dried (MgSO4) and concentrated in vacuo to an oil (0.9 g). The oil was purified by chromatography over silica gel eluting with a gradient of methanol/dichloromethane to afford an orange oil (0.28 g, Rf 0.11, methanol/dichloromethane 1:19). This material was further purified by passage through a strong cation exchange (SCX) column eluting firstly with methanol (fractions discarded) and then with methanol/aqueous ammonia-880 (10:1) to give the title compound (E1) as an orange oil (0.152 g, 0.41 mmol, 7% over two steps);

후처리

  1. temperatureTo the reaction mixture, cooled to ambient temperature
  2. filtrationThe insoluble material was filtered
  3. washwashed with dichloromethane (3×20 ml)
  4. customThe filtrate and washings were transferred to a separating funnel
  5. customthe layers separated
  6. extractionThe aqueous layer was extracted with dichloromethane (100 ml)
  7. washthe combined organic extracts were washed with water (100 ml)
  8. dry with materialdried (MgSO4)
  9. concentrationconcentrated in vacuo to an oil (0.9 g)
  10. customThe oil was purified by chromatography over silica gel eluting with a gradient of methanol/dichloromethane
  11. customto afford an orange oil (0.28 g, Rf 0.11, methanol/dichloromethane 1:19)
  12. customThis material was further purified by passage through a strong cation exchange (SCX) column
  13. washeluting firstly with methanol (fractions discarded)

출처 및 근거

ORD 기록
ord-cc38edef63f141558aa66e6471a9b3f5
출처 데이터셋
uspto-grants-2008_11
특허 번호
US07452888B2

연결된 노트

불러오는 중…