반응 #88319

ord-f1df7ed542cf4c39a393af7f90a4d2ef

반응 방정식

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

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.ADDITIONis added dropwise
  2. 2
    농축concentrated in vacuo
  3. 3
    workup.DISSOLUTIONThe resulting residue is dissolved in EtOAc
  4. 4
    세척washed with 1N HCl and brine
  5. 5
    건조The solution is dried over Na2SO4
  6. 6
    여과filtered
  7. 7
    농축concentrated
  8. 8
    기타the crude material purified over silica

실험 절차

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.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US09440963B2uspto-grants-2016_09