Water → HCID 69735448, 화합물

HRID 586215노트

반응식

HRID 586215 반응식
[NH:1]1[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.C(N(CC)CC)C.Cl[C:15]1[CH:16]=[CH:17][C:18]2[O:22][C:21]([S:23](Cl)(=[O:25])=[O:24])=[CH:20][C:19]=2[CH:27]=1.O.[Cl:29]CCl>C(OCC)C>[Cl:29][CH:2]1[CH2:3][N:4]([S:23]([C:21]2[O:22][C:18]3[CH:17]=[CH:16][CH:15]=[CH:27][C:19]=3[CH:20]=2)(=[O:24])=[O:25])[CH2:5][CH2:6][NH:1]1

참가 물질

7

실험 절차

A stirred solution of piperazine (1.15 g, 13.4 mmol) and triethylamine (4.7 ml, 46.5 mmol) in dichloromethane (30 ml) was cooled to ˜5° C. and a solution of 5-chlorobenzofuran-2-sulphonyl chloride (1.69 g, 7.8 mmol) in dichloromethane (10 ml) was added. Stirring was continued for 15 mins, and the reaction mixture then allowed to warm to ambient temperature over 2 hrs with stirring. Water was added to the reaction mixture, and the organic layer separated; this was washed with water (twice), brine (once), then dried (MgSO4), filtered and evaporated to give a yellow gum. This was chromatographed (Merck Art 9385 silica, eluting with dichloromethane containing increasing amounts of methanol, up to 10% v/v) to give a yellow solid; trituration with diethyl ether gave 5-chlorobenzofuran-2-ylsulphonyl piperazine as a colourless solid (1.11 g) which was used without further purification, 1H NMR (CDCl3) δ=2.8-3.0 ppm (t, 4H), δ=3.2-3.4 ppm (t, 4H), δ=7.3 ppm (s, 1H), δ=7.45 ppm (dd, 2H), δ=7.7 ppm (s, 1H); MS (M+H)+ 301/303.

후처리

  1. stirringwith stirring
  2. customthe organic layer separated
  3. washthis was washed with water (twice), brine (once),
  4. dry with materialthen dried (MgSO4)
  5. filtrationfiltered
  6. customevaporated
  7. customto give a yellow gum
  8. customThis was chromatographed (Merck Art 9385 silica
  9. washeluting with dichloromethane containing
  10. temperatureincreasing amounts of methanol
  11. customup to 10% v/v) to give a yellow solid

출처 및 근거

ORD 기록
ord-c81d95c249304e6d92e7bf25941604ce
출처 데이터셋
uspto-grants-2005_08
특허 번호
US06936610B2

반응 노트

불러오는 중…