A kind of chromeno[2,3-b]quinoline derivative and its preparation method and application

A derivative, 3-b technology, applied in the direction of drug combination, organic chemistry, antineoplastic drugs, etc., can solve the problems of cytotoxic activity and other problems, achieve the effect of simple and convenient process route, inhibit tumor cell growth, and inhibit proliferation in vitro

Active Publication Date: 2019-02-19
JIANGSU UNIV OF TECH
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  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

Recently, it has been reported in the literature that derivatives such as chromenoquinolines with a spiro ring structure have good antitumor activity, and the results show that this type of compound has cytotoxic activity against breast cancer and cervical cancer.

Method used

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  • A kind of chromeno[2,3-b]quinoline derivative and its preparation method and application
  • A kind of chromeno[2,3-b]quinoline derivative and its preparation method and application
  • A kind of chromeno[2,3-b]quinoline derivative and its preparation method and application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0019] Add 2-chloroquinoline-3-carbaldehyde (0.2mmol), malononitrile (0.2mmol) and 5,5-dimethyl-1,3-cyclohexanedione (0.2mmol) into a 5mL microwave reaction tube, Then add L-proline (0.1mmol) and ethanol 2mL, seal the reaction tube, stir for 10 seconds in advance, and react the mixture at 100°C for 30 minutes under microwave radiation. After the reaction, cool the reaction system to room temperature and wait for precipitation Suction filtration after the solid, and then recrystallization with a mixed solvent of DMF and water to obtain 2-(3,3-dimethyl-1-oxo-2,3,4,12-tetrahydro-1H-chromene and [2,3-b]quinolin-12-yl)malononitrile (Ia): Yield 71%; m.p.: 248-250°C; IR (KBr, ν, cm -1 ):3047,2920,2254,1622,1598,1448,1399,1215,1091,1055,1027,999,752,689; 1 H NMR (400MHz, DMSO-d 6 )(δ,ppm):8.71(s,1H,ArH),8.07(d,J=7.6Hz,1H,ArH),7.94(d,J=8.4Hz,1H,ArH),7.88-7.84(m, 1H, ArH), 7.67-7.63(m, 1H, ArH), 5.23(d, J=4.0Hz, 1H, CH), 5.00(d, J=4.0Hz, 1H, CH), 2.81(d, J= 18.0Hz,1H,CH),2.68(d,J=18...

Embodiment 2

[0021] According to the method for embodiment 1, 2-chloroquinoline-3-formaldehyde is changed into 6-methoxyl group-2-chloroquinoline-3-formaldehyde, with L-proline as catalyst, reacted under microwave radiation for 30 minutes, Recrystallization with a mixed solvent of DMF and water gave the target product 2-(9-methoxy-3,3-dimethyl-1-oxo-2,3,4,12-tetrahydro-1H-chromeno [2,3-b]quinolin-12-yl)malononitrile (Ib): 74% yield; m.p.: 268-270°C; IR (KBr, ν, cm -1 ):2896,2254,1635,1613,1466,1356,1238,1216,1142,1112,1029,834; 1 H NMR (400MHz, DMSO-d 6 )(δ,ppm):8.57(s,1H,ArH),7.84(d,J=9.2Hz,1H,ArH),7.51-7.48(m,1H,ArH),7.45(d,J=2.4Hz, 1H, ArH), 5.20(d, J=4.0Hz, 1H, CH), 4.97(d, J=3.6Hz, 1H, CH), 3.93(s, 3H, CH 3 O), 2.79(d, J=17.6Hz, 1H, CH), 2.65(d, J=17.2Hz, 1H, CH), 2.45(d, J=16.4Hz, 1H, CH), 2.33(d, J =16.4Hz,1H,CH),1.15(s,3H,CH 3 ),1.13(s,3H,CH 3 ).

Embodiment 3

[0023] According to the method for Example 1, 2-chloroquinoline-3-formaldehyde is replaced with 6-tert-butyl-2-chloroquinoline-3-formaldehyde, and L-proline is used as a catalyst to react under microwave radiation for 30 minutes. Recrystallization with a mixed solvent of DMF and water gave the target product 2-(9-tert-butyl-3,3-dimethyl-1-oxo-2,3,4,12-tetrahydro-1H-chromene [2,3-b]quinolin-12-yl)malononitrile (Ic): 75% yield; m.p.: 228-230°C; IR (KBr, ν, cm -1 ):2960,2937,2254,1642,1611,1439,1394,1346,1265,1236,1212,1174,1145,1118,1024,997,831; 1 HNMR (400MHz, DMSO-d 6 )(δ,ppm):8.68(s,1H,ArH),8.01-7.89(m,3H,ArH),5.25(d,J=3.6Hz,1H,CH),4.99(d,J=3.6Hz, 1H, CH), 2.81(d, J=18.0Hz, 1H, CH), 2.52(d, J=18.8Hz, 2H, CH 2 ), 2.36(d, J=16.0Hz, 1H, CH), 1.41(s, 9H, (CH 3 ) 3 C).

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Abstract

A chromeno[2,3-b]quinoline derivative, its structural formula is as shown in I: wherein, R1 is any one of H, CH3O, Cl or (CH3)3C; R2 is H or CH3 ; R3 is H, CH3 or Ph. The derivative is synthesized in one step using 2-chloroquinoline-3-formaldehyde or its derivative, malononitrile and 1,3-cyclohexanedione or its derivative as raw materials. The synthetic process route is simple, the conditions are mild, and the total yield is over 61%. The compound provided by the invention has been proved by pharmacological experiments that it has a good in vitro anti-proliferation effect on the human liver tumor cell line HepG2, has the effect of inhibiting the growth of tumor cells, and can be used in the preparation of anti-tumor drugs.

Description

technical field [0001] The invention belongs to the technical field of organic synthesis, and relates to a preparation method of chromeno[2,3-b]quinoline derivatives and their application in antitumor drugs Background technique [0002] Chromene, also known as benzopyran, its skeleton widely exists in natural products, for example, vitamin E, flavonoids, isoflavones, etc. all contain chromene skeleton. Chromene derivatives have a wide range of biological and pharmacological activities. There have been reports of anti-allergic and anti-cancer activities. [0003] Quinoline, also known as benzopyridine or aziridine, is a very important class of nitrogen-containing heterocyclic compounds, especially in the pharmaceutical industry and has a wide range of applications. Moreover, they are also the mother nucleus of the structure of many natural products and bioactive drugs, such as: chloroquine, camelline, camptothecin. After continuous research by pharmacologists, a large numb...

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): C07D491/052A61P35/00
CPCC07D491/052
Inventor 林伟蔡琦胡秀秀王雅珍王赟
Owner JIANGSU UNIV OF TECH
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