تفاعل #989

ord-696b27b131f24c17a8f31b09f5726b28

معادلة التفاعل

C[C@H](CO)Nc1ccccn1
(R)-N-(2-pyridyl)-2-aminopropanol
CCN(C(C)C)C(C)C
N,N-diisopropylethylamine
O=S(Cl)Cl
thionyl chloride
CC1CO[S@@](=O)N1c1ccccn1
(R)-4-methyl-3-(2-pyridyl)-[1,2,3] oxathiazolidine 2-oxide

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىwas kept below 10° C
  2. 2
    أخرىThe organic phase was separated
  3. 3
    غسيلwashed with water (5×500 ml)
  4. 4
    استخلاصThe aqueous phase was back-extracted with dichloromethane (2×500 ml)
  5. 5
    تجفيفdried (MgSO4)
  6. 6
    أخرىevaporated in vacuo
  7. 7
    أخرىto give a brown oil
  8. 8
    أخرىThis was purified on a silica column
  9. 9
    غسيلeluting with diethyl ether

الإجراء التجريبي

A solution of (R)-N-(2-pyridyl)-2-aminopropanol (20.0 g, 0.13 moles) and N,N-diisopropylethylamine (33.6 g, 0.13 moles) in dichloromethane (500 ml) was cooled to 5° C. Then thionyl chloride (15.5 g, 0.13 moles) in dichloromethane (100 ml) was added slowly whilst the temperature was kept below 10° C. The mixture was stirred for 0.5 h. and ice cold water (500 ml) was added. The organic phase was separated and washed with water (5×500 ml). The aqueous phase was back-extracted with dichloromethane (2×500 ml), the organic phases were combined, dried (MgSO4) and evaporated in vacuo to give a brown oil. This was purified on a silica column, eluting with diethyl ether to give (R)-4-methyl-3-(2-pyridyl)-[1,2,3] oxathiazolidine 2-oxide (154.4 g) as a clear oil.

المصدر

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