반응 #813860

ord-133921d3769d43b396cb6509f7f861d0

반응 방정식

O=C(O)c1c(-c2ccc3c(c2)OCO3)c2ccccc2[nH]c1=O
1,2-dihydro-4-(3,4-methylenedioxyphenyl)-2-oxo-3-quinoline carboxylic acid
O=P(Cl)(Cl)Cl
phosphorous oxychloride
O=C1c2cc3c(cc2-c2c1c(Cl)nc1ccccc21)OCO3
title compound
수율 59.9%
O=C1c2cc3c(cc2-c2c1c(Cl)nc1ccccc21)OCO3
6-chloro-9,10-methylenedioxy-7H-indeno[2,1-c]quinoline-7-on
수율 59.9%

반응 조건

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

후처리

  1. 1
    온도was refluxed
  2. 2
    온도with heat for 4 hours
  3. 3
    workup.DISTILLATIONThe reaction mixture was distilled to dryness
  4. 4
    세척washed with n-hexane several times
  5. 5
    기타To the residue obtained
  6. 6
    기타precipitated
  7. 7
    기타The crystal obtained
  8. 8
    여과to filter off undissolved substances
  9. 9
    기타purified by silica gel column chromatography (eluent: chloroform)

실험 절차

A mixture of 1,2-dihydro-4-(3,4-methylenedioxyphenyl)-2-oxo-3-quinoline carboxylic acid obtained in reference example 1 (10 g, 32.3 mmol) and phosphorous oxychloride (100 ml, 1.07 mol) was refluxed with heat for 4 hours. The reaction mixture was distilled to dryness and washed with n-hexane several times. To the residue obtained was added 50 g of polyphosphoric acid, and the mixture was heated at 90° C. for 2 hours. The reaction mixture was poured into ice water to filtrate a crystal precipitated. The crystal obtained was dissolved in tetrahydrofuran to filter off undissolved substances, and purified by silica gel column chromatography (eluent: chloroform) to give 6.0 g (yield 59.9%) of the title compound.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US05710162uspto-grants-1998_01