تفاعل #685029

ord-95c278858c9f48bda48c0567547822f6

معادلة التفاعل

C1CCNCC1
piperidine
CCOC(=O)CCc1c(C=O)[nH]c2c1C(=O)CCC2
compound 5
CCOC(=O)CCc1c(C=O)[nH]c2c1C(=O)CCC2
3-(3-Ethoxy-3-oxopropyl)-2-formyl-4-oxo-4,5,6,7-tetrahydro-1H-indole
O=C1Cc2ccccc2N1
indolin-2-one
CCOC(=O)CCc1c(/C=C2\C(=O)Nc3ccccc32)[nH]c2c1C(=O)CCC2
(Z)-3-((3-(3-ethoxy-3-oxopropyl)-4-oxo-4,5,6,7-tetrahydro-1H-indol-2-yl)methylene)indolin-2-one

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    درجة الحرارةThe reaction was heated
  2. 2
    درجة الحرارةat reflux for 12 h
  3. 3
    ترشيحThe resultant precipitate was filtered
  4. 4
    غسيلwashed with EtOH
  5. 5
    أخرىto provide the diresed product

الإجراء التجريبي

A mixture of compound 5 (0.50 mmol) and indolin-2-one (0.50 mmol) was added with EtOH (5.0 mL) and piperidine (0.1 mL). The reaction was heated at reflux for 12 h. The resultant precipitate was filtered and washed with EtOH to provide the diresed product. 1H NMR (CDCl3) δ 7.93 (s, 1 H), 7.61 (s, 1 H), 7.59 (d, 1 H, ArH), 7.19 (dd, 1 H), 7.09 (dd, 1 H), 6.89 (d, 1 H), 4.07 (q, 2 H), 3.27 (t, 2 H), 2.91 (t, 2 H), 2.74 (t, 2 H), 2.52 (t, 2 H), 2.14-2.19 (m, 2 H), 1.18 (t, 3 H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07897602B2uspto-grants-2011_03