반응 #685029

ord-95c278858c9f48bda48c0567547822f6

반응 방정식

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

용매

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The reaction was heated
  2. 2
    온도at reflux for 12 h
  3. 3
    여과The resultant precipitate was filtered
  4. 4
    세척washed with EtOH
  5. 5
    기타to provide the diresed product

실험 절차

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).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07897602B2uspto-grants-2011_03