تفاعل #88319

ord-f1df7ed542cf4c39a393af7f90a4d2ef

معادلة التفاعل

CCc1csc([C@@H](N)Cc2ccc([N+](=O)[O-])cc2)n1
(S)-1-(4-ethylthiazol-2-yl)-2-(4-nitrophenyl)ethanamine
Cn1ccnc1
N-methyl imidazole
O=C(O)CCC(=O)c1ccccc1
3-Benzoylpropionic acid
O=S(Cl)Cl
thionyl chloride
CCc1csc([C@H](Cc2ccc([N+](=O)[O-])cc2)NC(=O)CCC(=O)c2ccccc2)n1
desired product
CCc1csc([C@H](Cc2ccc([N+](=O)[O-])cc2)NC(=O)CCC(=O)c2ccccc2)n1
(S)—N-[1-(4-ethylthiazol-2-yl)-2-(4-nitrophenyl)ethyl]-4-oxo-4-phenylbutanamide

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONis added dropwise
  2. 2
    تركيزconcentrated in vacuo
  3. 3
    workup.DISSOLUTIONThe resulting residue is dissolved in EtOAc
  4. 4
    غسيلwashed with 1N HCl and brine
  5. 5
    تجفيفThe solution is dried over Na2SO4
  6. 6
    ترشيحfiltered
  7. 7
    تركيزconcentrated
  8. 8
    أخرىthe crude material purified over silica

الإجراء التجريبي

3-Benzoylpropionic acid (0.250 g) is dissolved in CH2Cl2 (5 mL), N-methyl imidazole (0.333 mL) is added and the resulting solution is cooled to 0° C. after which a solution of thionyl chloride (0.320 g) in CH2Cl2 (2 mL) is added dropwise. After 0.5 hours (S)-1-(4-ethylthiazol-2-yl)-2-(4-nitrophenyl)ethanamine, 3, (0.388 g) is added. The reaction is stirred for 18 hours at room temperature and then concentrated in vacuo. The resulting residue is dissolved in EtOAc and washed with 1N HCl and brine. The solution is dried over Na2SO4, filtered, and concentrated and the crude material purified over silica to afford 0.415 g of the desired product.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09440963B2uspto-grants-2016_09