تفاعل #51457

ord-a2134bdda9f04a9197d3c49f090a8b58

معادلة التفاعل

NCCCN
1,3-diaminopropane
O=S(=O)(Cl)c1ccc(Oc2ccc(F)cc2)cc1
4-(4-fluorophenoxy)benzenesulfonyl chloride
NCCCNS(=O)(=O)c1ccc(Oc2ccc(F)cc2)cc1
N-(3-aminopropyl)-4-(4-fluorophenoxy)benzenesulfonamide

الكواشف

لا شيء

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONafter the addition
  2. 2
    أخرىpartitioned between ethyl acetate and water
  3. 3
    workup.ADDITIONThe resulting emulsion was cleared by addition of dichloromethane
  4. 4
    أخرىthe organic layer was separated
  5. 5
    استخلاصThe aqueous layer was extracted with dichloromethane
  6. 6
    استخلاصthe combined organic layers were extracted with 0.5 N aq. sodium bisulfate
  7. 7
    استخلاصextracted with dichloromethane (3×100 mL)
  8. 8
    تجفيفThe combined organic layers were dried over sodium sulfate
  9. 9
    تركيزconcentrated to a volume of about 50 mL
  10. 10
    workup.ADDITIONAddition of hexane resulting in formation of a precipitate, which
  11. 11
    ترشيحwas collected by filtration

الإجراء التجريبي

To a stirred solution of 1,3-diaminopropane (6.7 mL) in 100 mL of dichloromethane at −10° C. was slowly added over a 2 hour period a solution of 4-(4-fluorophenoxy)benzenesulfonyl chloride (5.7 g, 20 mmol) in 50 mL of dichloromethane. The reaction was stirred for 15 minutes after the addition was complete, and then partitioned between ethyl acetate and water. The resulting emulsion was cleared by addition of dichloromethane, and the organic layer was separated. The aqueous layer was extracted with dichloromethane and the combined organic layers were extracted with 0.5 N aq. sodium bisulfate. The aqueous phase was brought to pH 8 with sodium bicarbonate and then extracted with dichloromethane (3×100 mL). The combined organic layers were dried over sodium sulfate and concentrated to a volume of about 50 mL. Addition of hexane resulting in formation of a precipitate, which was collected by filtration to provide N-(3-aminopropyl)-4-(4-fluorophenoxy)benzenesulfonamide (4.27 g) as a white solid: mp 184° C. (softens), 237° C. (melts) 1H NMR (300 MHz, DMSO-d6): δ 7.84 (d, J=9 Hz, 2H), 7.38-7.21 (m, 4H), 7.12 (d, J=9 Hz, 2H), 3.6-3.2 (br s, 3H), 2.80 (dd, J=7, 7 Hz, 2H), 2.77 (dd, J=7, 7 Hz, 2H), 1.72-1.60 (m, 2H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US06849732B2uspto-grants-2005_02