تفاعل #991

ord-094501f6e5574d25af8d8557ebfc848e

معادلة التفاعل

C[C@@H]1COS(=O)(=O)N1c1ccccn1
(R)-4-methyl-3-pyridin-2-yl-[1,2,3]-oxathiazolidine-2,2-dioxide
c1cc(N2CCNCC2)c2cc[nH]c2c1
4-piperazinoindole
C[C@H](CN1CCN(c2cccc3[nH]ccc23)CC1)Nc1ccccn1
(R)-1-(4-indolyl)-4-[2-methyl-2-(2-pyridinylamino)ethyl]piperazine
المردود 67.5%

المذيبات

ظروف التفاعل

درجة الحرارة
60°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىthen evaporated in vacuo
  2. 2
    درجة الحرارةcooled
  3. 3
    غسيلwashed with ethyl acetate (2×100 ml)
  4. 4
    استخلاصextracted into dichioromethane (3×100 ml)
  5. 5
    تجفيفdried (MgSO4)
  6. 6
    أخرىthen evaporated in vacuo
  7. 7
    أخرىto give a brown glass
  8. 8
    أخرىThis was purified on a silica column
  9. 9
    غسيلeluting with 10% propan-2-ol in dichloromethane

الإجراء التجريبي

A solution of (R)-4-methyl-3-pyridin-2-yl-[1,2,3]-oxathiazolidine-2,2-dioxide (4.04 g 0.019 moles) and 4-piperazinoindole (3.80 g 0.019 moles) in acetonitrile (200 ml) was heated to 60° C. for 0.5 h then evaporated in vacuo. The residue was taken up into dilute HCl (100 ml), warmed to 60° C. for 0.5 h, cooled, washed with ethyl acetate (2×100 ml), made basic with potassium carbonate, extracted into dichioromethane (3×100 ml), dried (MgSO4) then evaporated in vacuo to give a brown glass. This was purified on a silica column eluting with 10% propan-2-ol in dichloromethane to give (R)-1-(4-indolyl)-4-[2-methyl-2-(2-pyridinylamino)ethyl]piperazine (4.3 g) as a clear glass.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05723464uspto-grants-1998_03