반응 #59368

ord-007e2dcc42ed49c4ba2ee43329806979

반응 방정식

O=C([O-])[C@H](O)[C@@H](O)C(=O)[O-].[K+].[Na+]
Rochelle's salt
CCNC(=O)C(C#N)=NNc1ccccc1Br
2-[(2-bromophenyl)-hydrazono]-N-ethyl-2-cyanoacetamide
[Al+3].[Cl-].[Cl-].[Cl-]
aluminum chloride
CCNC(=O)c1nnc2c(Br)cccc2c1N
title compound
수율 69.3%
CCNC(=O)c1nnc2c(Br)cccc2c1N
4-Amino-8-bromo-N-ethyl-cinnoline-3-carboxamide
수율 69.3%

반응 조건

온도
90°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    온도The reaction was heated
  2. 2
    온도cooled
  3. 3
    workup.STIRRINGAfter stirring for 30 minutes
  4. 4
    기타the organic layer was decanted into a separator funnel
  5. 5
    세척(The white precipitate was rinsed with ethyl acetate three times
  6. 6
    세척) The organic layer was washed with 1:1 brine
  7. 7
    건조Rochelle's salt solution, dried over sodium sulfate
  8. 8
    농축concentrated to a light brown solid
  9. 9
    여과filtered

실험 절차

To a stirred solution of 2-[(2-bromophenyl)-hydrazono]-N-ethyl-2-cyanoacetamide (260 mg, 0.88 mmol) in anhydrous toluene (10 mL) was added aluminum chloride (370 mg, 2.78 mmol). The reaction was heated with vigorous stirring at 90° C. for 1.5 hours, cooled, diluted with ethyl acetate (40 mL), and treated with Rochelle's salt (saturated aqueous solution). After stirring for 30 minutes, the organic layer was decanted into a separator funnel. (The white precipitate was rinsed with ethyl acetate three times.) The organic layer was washed with 1:1 brine:Rochelle's salt solution, dried over sodium sulfate, and concentrated to a light brown solid. The solid was slurred in ether and filtered to afford the title compound as a brown solid (180 mg, 69%). 1H NMR (300.132 MHz, CDCl3) δ 8.52 (s, 1H), 8.13 (dd, J=7.4, 1.1 Hz, 1H), 7.82 (dd, J=8.4, 1.1 Hz, 1H), 7.51 (dd, J=8.4, 7.5 Hz, 1H), 3.56 (dq, J=5.8, 7.3 Hz, 2H), 1.31 (t, J=7.3 Hz, 3H). MS APCI, m/z=395/397 (M+H). HPLC 1.90 min.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07425556B2uspto-grants-2008_09