تفاعل #69358

ord-0ae50bad8b584d56bbc35aa982d42625

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.DISSOLUTIONdissolves
  2. 2
    ترشيحThe precipitate (desired product) is filtered off
  3. 3
    غسيلwashed three times with diethyl ether
  4. 4
    أخرىdried
  5. 5
    تركيزThe combined mother liquors are concentrated under reduced pressure
  6. 6
    درجة الحرارةrefluxed for 13 h (the precipitate
  7. 7
    workup.DISSOLUTIONdissolves
  8. 8
    ترشيحThe precipitate (desired product) is filtered off
  9. 9
    غسيلwashed three times with diethyl ether
  10. 10
    أخرىdried

الإجراء التجريبي

A suspension of 2-[(2S)-2-oxiranylmethyl]-1H-isoindole-1,3(2H)-dione (A. Gutcait et al. Tetrahedron Asym. 1996, 7, 1641) (5.68 g, 27.9 mmol) and 4-(4-aminophenyl)-3-morpholinone (5.37 g, 27.9 mmol) in ethanol/water (9:1, 140 ml) is refluxed for 14 h (the precipitate dissolves, after some time again formation of a precipitate). The precipitate (desired product) is filtered off, washed three times with diethyl ether and dried. The combined mother liquors are concentrated under reduced pressure and, after addition of a second portion of 2-[(2S)-2-oxiranylmethyl]-1H-isoindole-1,3(2H)-dione (2.84 g, 14.0 mmol), suspended in ethanol/water (9:1, 70 ml) and refluxed for 13 h (the precipitate dissolves, after some time again formation of a precipitate). The precipitate (desired product) is filtered off, washed three times with diethyl ether and dried. Total yield: 10.14 g, 92% of theory.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08530505B2uspto-grants-2013_09