KR20110080660A - Environmental friendly synthesis method of spirooxyindole derivatives - Google Patents
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- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
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- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
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Abstract
Description
The present invention relates to an environmentally friendly synthesis method capable of synthesizing spirooxyindole derivatives quickly, simply and efficiently in a single step process.
Molecules with spirooxyindole groups are widely found in nature and are known to have important physiological activities. Due to its unique structural arrangement and excellent pharmacological activity, much attention has been paid to the synthesis of spirooxyindole derivatives.
Several methods for the synthesis of spirooxyindole derivatives have been known so far, but there are no reports on the rapid, easy and environmentally friendly synthesis.
Therefore, there is a need for the development of a new and simple method for the synthesis of spirooxyindole derivatives having a wide range of physiological activities and properties.
An object of the present invention is to develop an eco-friendly method for synthesizing spirooxyindole derivatives simply, quickly and efficiently.
In order to achieve the above object,
The present invention is spirooxy, characterized in that the isatin, malononitrile and 1,3-dicarbonyl compound in water in the presence of ethylenediamine diacetate to prepare any one compound selected from the following formulas (1) to (3) Provided are methods for the synthesis of indole derivatives:
In Chemical Formulas 1 to 3, the R, R 1 And R 2 is hydrogen, halogen or alkyl, R 3 is hydrogen, alkyl, phenyl, said R 4 and R 5 are hydrogen or alkyl and n is an integer from 0 to 1.
The 1,3-dicarbonyl compound is 5,5-dimethylcyclohexane-1,3-dione, cyclohexane-1,3-dione, 5-isopropylcyclohexane-1,3-dione, 5 -Phenylcyclohexane-1,3-dione, 3-hydroxy- 1H -phenal-1-one, cyclopentane-1,3-dione, acyclic β-keto ester and 4-hydroxycoumarin It may be any one selected from the group.
More specifically, the present invention comprises the steps of preparing a mixture of isatin, malononitrile and 1,3-dicarbonyl compound in water; Adding ethylenediamine diacetate to the mixture; Stirring the reaction mixture at a temperature of 50 to 70 ° C. for 1 to 4 hours and then cooling to room temperature; And it provides a method for synthesizing the spirooxyindole derivative comprising the step of filtering, washing and drying the obtained material.
For example, a method for synthesizing a spiroxyoxyindole derivative according to the present invention is a mixture of 0.1-10 mmol of isatin, 0.1-10 mmol of malononitrile and 0.1-10 mmol of 1,3-dicarbonyl compound in 5 ml of water. Preparing a; Adding 0.01 to 1 mmol of ethylenediamine diacetate to the mixture at room temperature; Stirring the reaction mixture at a temperature of 50 to 70 ° C. for 1 to 4 hours and then cooling to room temperature; And filtering, washing, and drying the obtained material.
Hereinafter, an Example is given and this invention is demonstrated in detail.
In the present invention, water is used as a solvent in order to compensate for the disadvantages of the compounds such as organic solvents used in the past and to synthesize spirooxyindole derivatives in an environmentally friendly manner. That is, a reactant composed of isatin (1), malononitrile (2) and 1,3-dicarbonyl compound, for example, 5,5-dimethylcyclohexane-1,3-dione (3), as in Scheme 1. Compound 4 may be prepared by reacting in the presence of ethylenediamine diacetate (EDDA) in a solvent of water.
Scheme 1
Various kinds of isatin, malononitrile and 1,3-dicarbonyl compounds can be reacted as shown in Table 1a and FIG. 1b to obtain various spirooxyindole derivatives.
On the other hand, the synthesis of spirooxyindole (4) can be carried out by the domino Knoevenagel condensation reaction and Michael addition reaction, as shown in Scheme 2. That is, isatin (1) is first reacted with EDDA to obtain protonated isatin (36), and then the protonated isatin (36) is attacked by anions produced by malononitrile in the presence of EDDA. Isatilidene malononitrile (38) is obtained as a xenoevenagel condensation product. The intermediate 38 is then attacked by the enol of dimethone 3 in the presence of EDDA to produce another intermediate 39, followed by the keto-enol tautomer to produce the enol intermediate 40. The imine intermediate 41 is produced by the nucleophilic reaction of the hydroxyl group to the cyano group of the intermediate 40, and finally, the desired spirooxyindole (4) compound is obtained.
Scheme 2
In addition, the present invention can synthesize a spirooxyindole derivative through a one-step manufacturing process using the isatin, malononitrile and 4-hydroxycoumarin derivatives as shown in Scheme 3.
Scheme 3
Various spirinoxy indole derivatives can be obtained by reacting various kinds of isatin, malononitrile and 4-hydroxycoumarin as shown in Table 2 below.
Synthesis of spirooxyindole derivatives according to the present invention is performed by condensation, addition of Michael and ring of domino xenoevenagel using isatin, malononitrile and 1,3-dicarbonyl compounds as raw materials in the presence of EDDA in a water solvent. By synthesizing through the polymerization reaction, it is possible to synthesize spirooxyindole derivatives which are environmentally friendly, fast, simple and with good yield.
1 illustrates an example of a method for synthesizing spirooxyindole derivatives according to the present invention.
Hereinafter, the present invention will be described in more detail with reference to the following examples. However, the present invention is not limited by these examples.
All the examples below were carried out in an aqueous medium, using pre-coated silica gel plates (Art. 5554) with a fluorescence detector for TLC analysis, and flash column chromatography using silica gel 9385. 1 H and 13 C NMR analyzes using DMSO- d 6 as solvent and a Bruker Model ARX (300 and 75 MHz, respectively) analyzer. IR analysis was performed using a Jasco FTIR 5300 analyzer. HRMS analysis was performed at Korea Basic Science Institute using Jeol JMS 700 analyzer.
Example 1 Common Synthesis Method
Ethylenediamine diacetate (EDDA; 18.0 mg, 0.1 mmol) in a solution of isatin (1.0 mmol), malononitrile (1.0 mmol) and 1,3-dicarbonyl (1.0 mmol) in water (5.0 ml) Was added at room temperature. The reaction mixture was stirred at 60 ° C. for 1-2 hours and then cooled to room temperature. The solid reaction was filtered, washed with water (2 x 10.0 ml) and ethanol (5.0 ml) and dried in a vacuum oven to give a white powder as product.
Example 2 Preparation of Compound 4
Isatin (1; 147 mg, 1.0 mmol), malononitrile (2; 66 mg, 1.0 mmol), and 5,5-dimethylcyclohexane-1,3-dione (3; 140 mg) in water (10 ml) , 1.0 mmol) was reacted at 60 ° C. for 1 hour to obtain a solid compound 4 (302 mg, 90%).
mp> 300 ° C .; 1 H NMR (300 MHz, DMSO- d 6 ) δ 10.35 (1H, s, -NH), 7.18 (2H, s, -NH 2 ), 7.12-6.70 (4H, m), 2.55-2.43 (2H, m ), 2.14-1.99 (2H, m), 0.96 (3H, s), 0.93 (3H, s); 13 C NMR (75 MHz, DMSO- d 6 ) δ 194.7, 177.8, 164.0, 158.6, 141.9, 134.2, 128.0, 122.8, 121.5, 117.1, 110.6, 109.1, 57.4, 49.9, 46.7, 31.8, 27.4, 26.9; IR (KBr) 3361, 2198, 1720, 1658, 1468, 1217 cm -1 .
Example 3 Preparation of Compound 15
Isatin (1; 147 mg, 1.0 mmol), malononitrile (2; 66 mg, 1.0 mmol), and cyclohexane-1,3-dione (8; 112 mg, 1.0 mmol) in water (10 ml) The reaction was carried out at 60 ° C. for 1 hour to obtain a solid compound 15 (291 mg, 95%).
mp> 300 ° C .; 1 H NMR (300 MHz, DMSO- d 6 ) δ 10.37 (1H, s, -NH), 7.19 (2H, s, -NH 2 ), 7.16-6.75 (4H, m), 2.70-2.62 (2H, m ), 2.27-2.18 (2H, m), 1.97-1.88 (2H, m); 13 C NMR (75 MHz, DMSO- d 6 ) δ 195.4, 1787.5, 166.4, 159.0, 142.4, 134.9, 128.5, 123.6, 122.0, 117.7, 112.3, 109.5, 58.1, 47.3, 36.8, 27.2, 20.2; IR (KBr) 3341, 3295, 3176, 2198, 1711, 1679, 1656, 1617, 1468, 1350, 1216, 1012, 755 cm -1 .
Example 4 Preparation of Compound 16
Isatin (1; 147 mg, 1.0 mmol), malononitrile (2; 66 mg, 1.0 mmol) in water (10 ml), and 5-isopropyl-1,3-cyclohexanedione (9 ; 154 mg, 1.0 mmol) was reacted at 60 ° C. for 1 hour to obtain Compound 16 (341 mg, 90%) as a 1: 1 mixture of diastereomers.
mp 283-285 ℃; 1 H NMR (300 MHz, DMSO- d 6 ) δ 10.35 (1H, s, -NH), 7.16 (2H, s, -NH 2 ), 7.12-6.73 (4H, m), 2.64-2.42 (2H, m ), 2.23-1.99 (2H, m), 1.88-1.790 (1H, m), 1.58-1.51 (1H, m), 0.85 (3H, d, J = 6.9 Hz) and 0.82 (3H, d, J = 6.9 Hz); 13 C NMR (75 MHz, DMSO- d 6 ) of one isomer δ 195.1, 178.0, 165.9, 158.7, 142.0, 134.5, 128.2, 123.3, 121.5, 117.3, 111.6, 109.1, 57.4, 46.8, 38.2, 30.9, 30.5, 30.3, 19.3; 13 C NMR (75 MHz, DMSO- d 6 ) of other isomer δ 195.0, 178.0, 165.4, 158.7, 141.9, 134.3, 128.1, 123.2, 121.5, 111.4, 117.3, 109.1, 57.4, 46.8, 38.2, 30.8, 30.5, 30.3, 19.2; IR (KBr) 3305, 2195, 1703, 1667, 1340, 1213, 1049 cm −1 ; HRMS m / z (M + ) calcd for C 20 H 19 N 3 O 3 : 349.1426. Found: 349.1425.
Example 5 Preparation of Compound 17
Isatin (1; 147 mg, 1.0 mmol), malononitrile (2; 66 mg, 1.0 mmol), and 5-phenyl-1,3-cyclohexanedione (10 ; 188 mg, 1.0) in water (10 ml) mmol) was reacted at 60 ° C. for 1 hour to afford compound 17 (317 mg, 83%) as a 1: 1 mixture of diastereomers.
mp 295-297 ° C; 1 H NMR (300 MHz, DMSO- d 6 ) δ 9.85 (1H, s, -NH), 6.83-6.20 (11H, m), 2.31-1.76 (5H, m); 13 C NMR (75 MHz, DMSO- d 6 ) of one isomer δ 194.6, 178.4, 165.8, 165.2, 159.2, 142.8, 142.6, 134.9, 134.7, 128.9, 127.4, 123.8, 122.0, 117.8, 112.3, 109.6, 58.2, 47.3, 43.8, 38.0, 34.5; 13 C NMR (75 MHz, DMSO- d 6 ) of other isomer δ 194.6, 178.4, 165.8, 165.1, 159.1, 142.8, 142.5, 134.6, 134.6, 128.6, 127.3, 123.6, 122.0, 117.7, 112.2, 109.6, 58.0, 47.3, 43.7, 37.9, 34.3; IR (KBr) 3310, 2194, 1722, 1671, 1619, 1341, 1215 cm −1 ; FAB-HRMS m / z [M + H] + calcd for C 23 H 18 N 3 O 3 : 384.1348. Found: 384.1345.
Example 6 Preparation of Compound 18
Isatin (1; 147 mg, 1.0 mmol), malononitrile (2; 66 mg, 1.0 mmol) in water (10 ml), and 3-hydroxy-1 H -phenalen-1-one (11 ; 196) mg, 1.0 mmol) was reacted at 60 ° C. for 2 hours to obtain a solid compound 18 (351 mg, 90%).
mp> 300 ° C .; 1 H NMR (300 MHz, DMSO- d 6 ) δ 10.60 (1H, s, -NH), 8.43-6.87 (12H, m); 13 C NMR (75 MHz, DMSO- d 6 ) δ 183.3, 177.8, 161.8, 158.5, 157.8, 142.1, 135.3, 133.3, 132.6, 131.1, 129.6, 128.9, 128.0, 127.1, 126.9, 126.2, 123.1, 121.4, 120.7 , 120.3, 117.0, 109.0, 57.0, 47.6 IR (KBr) 3404, 2199, 1725, 1666, 1624, 1333, 1218 cm −1 ; HRMS m / z (M) + calcd for C 24 H 13 N 3 O 3 : 391.0957. Found: 391.0960.
Example 7 Preparation of Compound 19
Isatin (1; 147 mg, 1.0 mmol), malononitrile (2; in water (10 ml); 66 mg, 1.0 mmol), and cyclopentane-1,3-dione (12 ; 98 mg, 1.0 mmol) were reacted at 60 ° C. for 1 hour to obtain a solid compound 19 (269 mg, 92%).
mp> 300 ° C .; 1 H NMR (300 MHz, DMSO- d 6 ) δ 10.55 (1H, s, -NH), 7.48 (2H, s, -NH 2 ), 7.22-6.80 (4H, m), 2.82-2.80 (2H, m ), 2.37-2.35 (2H, m); 13 C NMR (75 MHz, DMSO- d 6 ) δ 199.7, 177.5, 176.6, 160.5, 142.0, 132.0, 128.8, 124.1, 121.9, 117.5, 114.8, 109.4, 56.4, 46.5, 33.1, 24.8; IR (KBr) 3347, 2195, 1718, 1665, 1346, 1232 cm −1 ; FAB-HRMS m / z [M + H] + calcd for C 16 H 12 N 3 O 3 : 294.0879. Found: 294.0882.
Example 8 Preparation of Compound 20
Isatin (1; 147 mg, 1.0 mmol), malononitrile (2; 66 mg, 1.0 mmol), and ethyl acetoacetate (13; 130 mg, 1.0 mmol) in water (10 ml) at 60 ° C. for 1 hour. Reaction was carried out to give a solid compound 20 (276 mg, 85%).
mp 255-256 ° C; 1 H NMR (300 MHz, DMSO- d 6 ) δ 10.35 (1H, s, -NH), 7.19-7.13 (1H, m), 7.09 (2H, s, -NH 2 ), 7.04-7.02 (1H, m ), 6.92 (1H, d, J = 7.8 Hz), 6.77 (1H, d, J = 7.5 Hz), 3.76 (2H, q, J = 6.3 Hz), 2.29 (3H, s), 0.77 (3H, t , J = 6.9 Hz); 13 C NMR (75 MHz, DMSO- d 6 ) δ 178.9, 164.9, 159.4, 158.8, 142.6, 134.9, 128.9, 123.8, 122.2, 117.8, 109.7, 105.1, 60.6, 57.1, 49.4, 18.9, 13.4; IR (KBr) 3473, 2193, 1719, 1676, 1620, 1471, 1377, 1288 cm −1 ; FAB-HRMS m / z [M + H] + calcd for C 17 H 16 N 3 O 4 : 326.1141. Found: 326.1141.
Example 9 Preparation of Compound 21
Isatin (1; 147 mg, 1.0 mmol), malononitrile (2; 66 mg, 1.0 mmol), and ethylbenzoyl acetate (14 ; 192 mg, 1.0 mmol) in water (10 ml) at 60 ° C. for 2 hours. Reaction was carried out to give solid compound 21 ((301 mg, 78%).
mp 261-263 ° C; 1 H NMR (300 MHz, DMSO- d 6 ) δ 9.62 (1H, s, -NH), 7.39-7.28 (8H, m), 7.13-7.08 (1H, m), 6.94-6.87 (1H, m), 6.79 (1H, d, J = 7.5 Hz), 3.62-3.55 (2H, q, J = 6.9 Hz), 0.57 (3H, t, J = 6.9 Hz); 13 C NMR (75 MHz, DMSO- d 6 ) δ 178.4, 164.9, 160.4, 155.7, 142.7, 133.5, 132.9, 130.7, 129.3, 128.7, 124.4, 122.4, 117.8, 109.9, 107.1, 60.7, 56.7, 50.2, 13.2 IR (KBr) 3470, 2195, 1720, 1670, 1380, 1220 cm −1 ; FAB-HRMS m / z [M + H] + calcd for C 22 H 18 N 3 O 4 : 388.1297. Found: 388.1299.
Example 10 Preparation of Compound 22
1-methylisatin (5; 161 mg, 1.0 mmol), malononitrile (2; 66 mg, 1.0 mmol), and cyclohexane-1,3-dione (8; 112 mg, 1.0 in water (10 ml) mmol) was reacted at 60 ° C. for 1 hour to obtain a solid compound 22 (272 mg, 85%).
mp 271-273 ° C; 1 H NMR (300 MHz, DMSO- d 6 ) δ 7.27-7.22 (1H, m), 7.18 (2H, s, -NH 2 ) 7.03-7.04 (1H, m), 6.99-6.94 (2H, m), 3.36 (3H, s), 2.68-2.64 (2H, m), 2.23-2.18 (2H, m), 1.94-1.90 (2H, m); 13 C NMR (75 MHz, DMSO- d 6 ) δ 194.7, 176.4, 165.9, 161.7, 158.6, 143.4, 133.4, 128.2, 122.7, 122.2, 117.0 107.9, 57.2, 46.4, 36.2, 26.6, 26.2, 19.6; IR (KBr) 3465, 2194, 1703, 1671, 1606, 1467, 1352, 1217 cm -1 .
Example 11 Preparation of Compound 23
1-methylisatin (5 ; 161 mg, 1.0 mmol), malononitrile ( 2; 66 mg, 1.0 mmol), and 5,5-dimethylcyclohexane-1,3-dione in water (10 ml) ; 140 mg, 1.0 mmol) for 60 ℃, by reacting for 1 hour, to give a compound of the solid 23 (293 mg, 84%) .
mp 264-266 ° C; 1 H NMR (300 MHz, DMSO- d 6 ) δ 7.27-7.22 (1H, m), 7.20 (2H, s, -NH 2 ), 7.05-6.95 (3H, m), 3.27 (3H, s), 2.50 (2H, s), 2.18-2.05 (2H, m), 1.03 (3H, s), 1.00 (3H, s); 13 C NMR (75 MHz, DMSO- d 6 ) δ 194.6, 176.4, 164.0, 158.7, 144.3, 143.5, 133.4, 128.2, 122.6, 122.2, 110.6, 108.0, 57.1, 49.9, 46.4, 31.8, 27.4, 27.0, 26.2 , 22.8; IR (KBr) 3441, 2194, 1686, 1608, 1468, 1352, 1219 cm -1 .
Example 12 Preparation of Compound 24
1-methylisatin (5 ; 161 mg, 1.0 mmol), malononitrile (2; 66 mg, 1.0 mmol), and 5-isopropyl-1,3-cyclohexane-dione (9 in water (10 ml) ; 154 mg, 1.0 mmol) for 60 ℃, part of isomers by reacting for 2 hours, 1: 1 as a mixture to give the compound 24 (294 mg, 81%) .
mp 256-258 ° C; 1 H NMR (300 MHz, DMSO- d 6 ) δ 7.27-7.22 (1H, m), 7.17 (2H, s), 7.08-6.96 (3H, m), 3.14 (3H, s), 2.68-2.55 (2H , m), 2.23-2.02 (2H, m), 1.90-1.88 (1H, m), 1.62-1.55 (1H, m), 0.89 (3H, d, J = 7.2 Hz) and (3H, d, J = 7.2 Hz); 13 C NMR (75 MHz, DMSO- d 6 ) δ 194.9, 176.3, 165.9, 165.4, 158.7, 143.5, 133.5, 128.2, 122.7, 122.1, 111.3, 107.9, 57.1, 46.4, 38.1, 30.7, 30.4, 30.2, 26.2 , 19.1; 3 C NMR (75 MHz, DMSO- d 6 ) of one isomer δ 194.9, 176.3, 165.9, 165.4, 158.7, 143.5, 133.5, 128.2, 122.8, 122.1, 111.5, 107.9, 57.1, 46.4, 38.1, 30.7, 30.4, 30.2, 26.2, 19.2 3 C NMR (75 MHz, DMSO- d 6 ) δ of other isomer 194.9, 176.3, 165.9, 165.4, 158.7, 143.4, 133.3, 128.2, 122.7, 122.1, 111.3, 107.9, 57.1, 46.4, 38.1 , 30.6, 30.4, 30.2, 26.2, 19.1; IR (KBr) 3394, 2196, 1675, 1609, 1488, 1342, 1212 cm −1 ; FAB-HRMS m / z [M + H] + calcd for C 21 H 22 N 3 O 3 : 364.1661. Found: 364.1664.
Example 13 Preparation of Compound 25
1-methylisatin (5; 161 mg, 1.0 mmol), malononitrile (2; 66 mg, 1.0 mmol), and 3-hydroxy-1 H -phenalen-1-one in water (10 ml) 11; 196 mg, 1.0 mmol) was reacted at 60 ° C. for 2 hours to obtain a solid compound 25 (303 mg, 75%).
mp> 300 ° C .; 1 H NMR (300 MHz, DMSO- d 6) δ 8.30-8.27 (6H, m), 7.91-7.73 (4H, m), 7.20-7.12 (2H, m), 3.14 (3H, s); 13 C NMR (75 MHz, DMSO- d 6 ) δ 181.0, 177.1, 159.4, 155.4, 144.3, 136.0, 133.6, 132.0, 131.8, 130.4, 129.0, 127.7, 127.1, 126.9, 125.3, 123.6, 122.9, 120.9, 117.7 , 113.3, 108.7, 105.9, 57.5, 47.9, 27.0; IR (KBr) 3358, 1722, 1574, 1515, 1473, 1227 cm −1 ; FAB-HRMS m / z [M + H] + calcd for C 25 H 16 N 3 O 3 : 406.1192. Found: 406.1195.
Example 14 Preparation of Compound 26
1-methylisatin (5; 161 mg, 1.0 mmol), malononitrile (2; 66 mg, 1.0 mmol), and cyclopentane-1,3-dione (12; 98 mg, 1.0 in water (10 ml) mmol) was reacted at 60 ° C. for 1 hour to obtain a solid compound 26 (270 mg, 88%).
mp 278-280 ° C; 1 H NMR (300 MHz, DMSO- d 6 ) δ 7.51 (2H, s, -NH 2 ), 7.33-7.28 (1H, m), 7.12 (1H, d, J = 7.2 Hz), 7.05-7.02 (2H , m), 3.15 (3H, s), 2.84-2.81 (2H, m), 2.37-2.34 (2H, m); 13 C NMR (75 MHz, DMSO- d 6 ) δ 200.5, 178.5, 176.0, 161.6, 144.3, 132.1, 129.9, 124.7, 123.6, 118.2, 115.6, 109.3, 57.0, 47.1, 34.0, 27.3, 25.7; IR (KBr) 3558, 2194, 1702, 1611, 1490, 1348, 1236 cm −1 ; FAB-HRMS m / z [M + H] + calcd for C 17 H 14 N 3 O 3 : 308.1035. Found: 308.1038.
Example 15 Preparation of Compound 27
5-methylisatin (6; 161 mg, 1.0 mmol), malononitrile (2; 66 mg, 1.0 mmol), and cyclohexane-1,3-dione (8; 112 mg, 1.0 in water (10 ml) mmol) was reacted at 60 ° C. for 1 hour to obtain a solid compound 27 (279 mg, 87%).
mp 292-293 ° C; 1 H NMR (300 MHz, DMSO- d 6 ) δ 10.22 (1H, s, -NH), 7.10 (2H, s, -NH 2 ), 6.93 (1H, d, J = 7.8 Hz), 6.81 (1H, s), 6.67 (1H, d, J = 7.8 Hz), 2.65 (2H, t, J = 5.5 Hz), 2.27-2.22 (2H, m), 2.21 (3H, s), 1.93 (2H, t, J = 6.0 Hz); 13 C NMR (75 MHz, DMSO- d 6 ) δ 194.7, 177.9, 165.7, 161.7, 158.4, 139.5, 134.5, 130.2, 128.2, 123.6, 111.9, 108.7, 57.8, 46.8, 36.3, 26.6, 20.5, 19.6; IR (KBr) 3360, 2196, 1705, 1661, 1349, 1212 cm −1 ; FAB-HRMS m / z [M + H] + calcd for C 18 H 16 N 3 O 3 : 322.1192. Found: 322.1194.
Example 16 Preparation of Compound 28
5-methylisatin (6; 161 mg, 1.0 mmol), malononitrile (2; 66 mg, 1.0 mmol), and 5-isopropyl-1,3-cyclohexanedione (9; 154 mg, 1.0 mmol) was reacted at 60 ° C. for 2 hours, to obtain Compound 28 (261 mg, 72%) as a 1: 1 mixture of partial isomers.
mp 275-276 ° C; 1 H NMR (300 MHz, DMSO- d 6 ) δ 10.24 (1H, s, -NH), 7.14 (2H, s, -NH), 6.93 (1H, d, J = 7.0 Hz), 6.82 (0.5 H, s) and 6.79 (0.5H, s), 6.66 (1H, d, J = 7.0 Hz), 2.68-2.50 (2H, m), 2.20 (3H, s), 2.17-2.08 (2H, m), 1.92- 1.84 (1H, m), 1.62-1.52 (1H, m), 0.89 (3H, d, J = 6.9 Hz) and 0.87 (3H, d, J = 6.9 Hz); 13 C NMR (75 MHz, DMSO- d 6 ) of one isomer δ 195.6, 178.5, 166.3, 159.1, 140.0, 135.0, 130.8, 128.9, 124.3, 117.8, 112.1, 109.3, 58.2, 47.4, 38.6, 31.4, 31.3, 30.8, 21.1, 19.6; 13 C NMR (75 MHz, DMSO- d 6 ) of other isomer δ 195.4, 178.4, 165.9, 159.1, 139.9, 134.8, 130.8, 128.8, 124.1, 117.8, 111.9, 109.3, 58.2, 47.4, 38.6, 31.4, 31.3, 30.8, 21.1, 19.6; IR (KBr) 3442, 2197, 1710, 1672, 1342, 1213 cm −1 ; FAB-HRMS m / z [M + H] + calcd for C 21 H 22 N 3 O 3 : 364.1661. Found: 364.1664.
Example 17 Preparation of Compound 29
5-methylisatin (6 ; 161 mg, 1.0 mmol), malononitrile (2; 66 mg, 1.0 mmol) in water (10 ml), and 5,5-dimethylcyclohexane-1,3-dione (3 140 mg, 1.0 mmol) was reacted at 60 ° C. for 1 hour to obtain a solid compound 29 (314 mg, 90%).
mp 298-299 ° C; 1 H NMR (300 MHz, DMSO- d 6 ) δ 10.22 (1H, s, -NH), 7.11 (2H, s, -NH 2 ), 6.90 (1H, d, J = 7.6 Hz), 6.78 (1H, s), 6.68 (1H, d, J = 7.6 Hz), 2,28 (3H, s), 2.20 (2H, s), 2.08 (2H, s), 1.04 (3H, s), 1.02 (3H, s ); 13 C NMR (75 MHz, DMSO- d 6 ) δ 194.6, 177.8, 163.8, 161.7, 158.6, 139.5, 134.4, 130.3, 128.3, 123.4, 110.8, 108.8, 57.8, 50.0, 46.8, 31.8, 27.3, 27.1, 24.3 , 20.5; IR (KBr): 3367, 2190, 1710, 1660, 1352, 1221 cm -1 .
Example 18 Preparation of Compound 30
5-methylisatin (6 ; 161 mg, 1.0 mmol), malononitrile (2; 66 mg, 1.0 mmol), and cyclopentane-1,3-dione (12; 98 mg, 1.0 in water (10 ml) mmol) was reacted at 60 ° C. for 1 hour to obtain a solid compound 30 (270 mg, 88%).
mp> 300 ° C .; 1 H NMR (300 MHz, DMSO- d 6 ) δ 10.47 (1H, s, -NH), 7.48 (2H, s, -NH 2 ), 7.04 (1H, d, J = 7.8 Hz), 6.91 (1H, s), 6.76 (1H, d, J = 8.1 Hz), 2.86-2.84 (2H, m), 2.42-2.40 (2H, m), 2.26 (3H, s); 13 C NMR (75 MHz, DMSO- d 6 ) δ 200.2, 177.9, 177.1, 160.9, 140.0, 132.6, 131.3, 129.5, 125.1, 118.0, 115.4, 109.7, 57.2, 47.1, 33.6, 25.3, 21.0 IR (KBr) 3357, 2195, 1725, 1660, 1492, 1347, 1235 cm -1 ; FAB-HRMS m / z [M + H] + calcd for C 17 H 14 N 3 O 3 : 308.1035. Found: 308.1036.
Example 19 Preparation of Compound 31
5-bromoissatin (7; 226 mg, 1.0 mmol), malononitrile (2; 66 mg, 1.0 mmol), and cyclohexane-1,3-dione (8; 112 mg, 1.0 in water (10 ml) mmol) was reacted at 60 ° C. for 1 hour to obtain a solid compound 31 (334 mg, 87%).
mp 298-300 ° C; 1 H NMR (300 MHz, DMSO- d 6 ) δ 10.51 (1H, s, -NH), 7.32-7.16 (4H, m), 6.74 (1H, d, J = 8.2 Hz), 2.75-2.61 (2H, m), 2.35-2.18 (2H, m), 2.05-1.90 (2H, m); 13 C NMR (75 MHz, DMSO- d 6 ) δ 195.6, 178.2, 167.0, 159.2, 141.8, 137.4, 131.3, 126.5, 117.6, 113.8, 111.7, 111.5, 57.4, 47.6, 36.7, 27.2, 20.1; IR (KBr) 3360, 2190, 1715, 1673, 1474, 1349, 1216 cm -1 .
Example 20 Preparation of Compound 32
5-bromoissatin (7; 226 mg, 1.0 mmol), malononitrile (2; 66 mg, 1.0 mmol), and 5-isopropyl-1,3-cyclohexanedione (9; 154 mg, 1.0 mmol) was reacted at 60 ° C. for 2 hours, to obtain Compound 32 (312 mg, 73%) as a 1: 1 mixture of partial isomers.
mp 283-285 ° C; 1 H NMR (300 MHz, DMSO- d 6 ) δ 10.50 (1H, s, -NH), 7.30-7.18 (4H, m), 6.73 (1H, d, J = 8.4 Hz), 2.66-2.41 (2H, m), 2.24-2.06 (2H, m), 1.92-1.85 (1H, m), 1.58-1.50 (1H, m), 0.87 (3H, d, J = 6.9 Hz) and 0.85 (3H, d, J = 6.9 Hz); 13 C NMR (75 MHz, DMSO- d 6 ) of one isomer δ 195.0, 177.3, 166.1, 166.0, 158.4, 141.0, 136.5, 130.5, 125.8, 116.7, 112.9, 110.7, 56.5, 46.7, 37.7, 30.6, 30.4, 29.9, 18.9, 18.7; 13 C NMR (75 MHz, DMSO- d 6 ) of other isomer δ 194.8, 177.2, 166.1, 166.0, 158.4, 141.0, 136.3, 130.5, 125.7, 116.7, 112.9, 110.7, 56.5, 46.7, 37.7, 30.6, 30.4, 29.9, 18.9, 18.7 IR (KBr) 3310, 2197, 1733, 1668, 1613, 1472, 1216 cm −1 FAB-HRMS m / z [M + H] + calcd for C 20 H 19 BrN 3 O 3 : 428.0610. Found: 428.0613.
Example 21 Preparation of Compound 33
5-bromoissatin (7; 226 mg, 1.0 mmol), malononitrile (2; 66 mg, 1.0 mmol), and 5,5-dimethylcyclohexane-1,3-dione (3) in water (10 ml) 140 mg, 1.0 mmol) was reacted at 60 ° C. for 1 hour to obtain a solid compound 33 (368 mg, 89%).
mp> 300 ° C .; 1 H NMR (300 MHz, DMSO- d 6 ) δ 10.54 (1H, s, -NH), 7.36-7.32 (1H, m), 7.31 (2H, s), 7.22 (1H, s), 6.78 (1H, d, J = 8.2 Hz), 2.65-2.55 (2H, m), 2.21-2.16 (2H, m), 1.05 (6H, s); 13 C NMR (75 MHz, DMSO- d 6 ) δ 195.5, 178.1, 165.0, 159.3, 141.9, 137.2, 131.4, 126.4, 117.6, 113.8, 111.6, 110.6, 57.3, 50.4, 47.5, 32.4, 28.0, 27.6; IR (KBr) 3293, 2194, 1726, 1658, 1473, 1351, 1220 cm -1 .
Example 22 Preparation of Compound 34
5-bromoissatin (7; 226 mg, 1.0 mmol), malononitrile (2; 66 mg, 1.0 mmol), and 3-hydroxy-1 H -phenalen-1-one in water (10 ml) 11; 196 mg, 1.0 mmol) was reacted at 60 ° C. for 1 hour to obtain a solid compound 34 (398 mg, 85%).
mp> 300 ° C .; 1 H NMR (300 MHz, DMSO- d 6 ) δ 10.72 (1H, s, -NH), 8.50-8.40 (3H, m), 8.30-8.28 (1H, d, J = 7.2 Hz), 7.94-7.83 ( 2H, m), 7.57 (2H, s), 7.38-7.34 (2H, m), 6.86-6.83 (1H, d, J = 7.5 Hz); 13 C NMR (75 MHz, DMSO- d 6 ) δ 181.5, 178.6, 159.7, 156.1, 142.5, 137.8, 136.4, 134.4, 132.2, 131.9, 130.8, 130.7, 128.1, 127.6, 127.2, 125.8, 121.4, 118.0, 114.3 , 113.1, 112.1, 57.5, 48.9; IR (KBr) 3409, 2200, 1726, 1664, 1473, 1338, 1224 cm −1 ; FAB-HRMS m / z [M + H] + calcd for C 24 H 13 BrN 3 O 3 : 470.0140. Found: 470.0142.
Example 23 Preparation of Compound 35
5-bromoissatin (7; 226 mg, 1.0 mmol), malononitrile (2; 66 mg, 1.0 mmol), and cyclopentane-1,3-dione (12; 98 mg, 1.0 in water (10 ml) mmol) was reacted at 60 ° C. for 1 hour to obtain a solid compound 35 (331 mg, 89%).
mp> 300 ° C .; 1 H NMR (300 MHz, DMSO- d 6 ) δ 10.68 (1H, s, -NH), 7.54 (2H, s, -NH 2 ), 7.39-7.30 (2H, m), 6.80 (1H, d, J = 8.1 Hz), 2.81-2.80 (2H, m), 2.39-2.37 (2H, m); 13 C NMR (75 MHz, DMSO- d 6 ) δ 200.3, 178.4, 176.8, 161.1, 141.8, 134.8, 132.1, 127.6, 117.8, 114.8, 114.2, 111.9, 56.3, 47.2, 33.6, 25.4; IR (KBr) 3363, 2193, 1710, 1676, 1474, 1345, 1234 cm −1 ; FAB-HRMS m / z [M + H] + calcd for C 16 H 11 BrN 3 O 3 : 371.9984. Found: 371.9980.
Example 24 Preparation of Compound 45
Isatin (1; 147 mg, 1.0 mmol), malononitrile (2; 66 mg, 1.0 mmol), and 4-hydroxycoumarin (42; 1.0 mmol) in water (10 ml) at 60 ° C. for 1 hour. Reaction gave a solid compound 45 (328 mg, 92%).
mp> 300 ° C .; 1 H NMR (300 MHz, DMSO- d 6 ) δ 10.64 (1H, s, -NH), 7.94 (1H, d, J = 8.1 Hz), 7.78-7.73 (1H, m), 7.62 (2H, s, -NH 2 ), 7.55-7.46 (2H, m) , 7.19 (2H, d, J = 7.5 Hz), 6.95-6.90 (1H, m), 6.85 (1H, d, J = 7.2 Hz); 13 C NMR (75 MHz, DMSO- d 6 ) δ 177.4, 158.7, 158.5, 155.3, 152.2, 142.4, 133.8, 133.3, 129.1, 125.2, 124.3, 122.9, 122.3, 117.2, 116.8, 112.7, 109.7, 101.7, 57.4 , 47.9; IR (KBr) 3306, 2203, 1717, 1673, 1609, 1472, 1358, 1108 cm -1 .
Example 25 Preparation of Compound 46
Isatin (1; 147 mg, 1.0 mmol), malononitrile (2; 66 mg, 1.0 mmol), and 4-hydroxy-6-methylcoumarin (43; 176 mg, 1.0 mmol) in water (10 ml) The reaction was carried out at 60 ℃ for 1 hour to give a solid compound 46 (337 mg, 91%).
mp> 300 ° C .; 1 H NMR (300 MHz, DMSO- d 6 , 300 MHz) δ 10.64 (1H, s, -NH), 7.75 (1H, s), 7.60-7.57 (3H, m), 7.39 (1H, d, J = 8.4 Hz), 7.23-7.16 (2H, m), 6.95-6.90 (1H, m), 6.85 (1H, d, J = 7.5 Hz), 2.44 (3H, s); 13 C NMR (75 MHz, DMSO- d 6 ) δ 177.6, 166.0, 162.5, 158.9, 155.4, 152.1, 150.6, 142.6, 134.8, 133.8, 129.3, 124.4, 123.1, 122.6, 116.4, 112.5, 109.9, 101.8, 57.6, 48.1, 20.7; IR (KBr): 3280, 2195, 1705, 1665, 1625, 1360, 1220 cm -1 FAB-HRMS m / z [M + H] + calcd for C 21 H 14 N 3 O 4: 372.0984. Found: 372.0986.
Example 26 Preparation of Compound 47
Isatin (1; 147 mg, 1.0 mmol), malononitrile (2; 66 mg, 1.0 mmol), and 4-hydroxy-6,7-dimethylcoumarin (44; 190 mg, 1.0 in water (10 ml) mmol) was reacted at 60 ° C. for 1 hour to obtain a solid compound 47 (354 mg, 92%).
mp> 300 ° C .; 1 H NMR (300 MHz, DMSO- d 6 ) δ 10.62 (1H, s, -NH), 7.68 (1H, s), 7.57 (1H, s), 7.30 (1H, s), 7.23-7.14 (3H, m), 6.95-6.83 (2H, m), 2.35 (3H, s), 2.33 (3H, s); 13 C NMR (75 MHz, DMSO- d 6 ) δ 177.7, 166.2, 162.6, 158.9, 155.5, 150.9, 144.1, 142.6, 134.0, 133.6, 129.3, 124.3, 123.3, 122.6, 117.4, 110.3, 109.9, 100.8, 57.6 , 48.0, 20.2, 19.4; IR (KBr) 3202, 2199, 1706, 1668, 1624, 1468, 1361, 1064 cm −1 ; FAB-HRMS m / z [M + H] + calcd for C 22 H 16 N 3 O 4 : 386.1141. Found: 386.1145.
Example 27 Preparation of Compound 48
1-methylisatin (5; 161 mg, 1.0 mmol), malononitrile (2; 66 mg, 1.0 mmol), and 4-hydroxy-6-methylcoumarin (43; 176 mg, in water (10 ml) 1.0 mmol) was reacted at 60 ° C. for 1 hour to obtain a solid compound 48 (327 mg, 85%).
mp 299-300 ° C; 1 H NMR (300 MHz, DMSO- d 6 ) δ 7.76 (1H, s), 7.65-7.57 (3H, m), 7.40-7.23 (3H, m), 7.08-7.01 (2H, m), 3.17 (3H , s), 2.44 (3H, s); 13 C NMR (75 MHz, DMSO- d 6 ) δ 176.1, 166.0, 162.4, 158.8, 155.5, 150.7, 144.1, 134.8, 133.9, 132.7, 129.5, 124.2, 123.2, 122.6, 116.8, 112.5, 108.9, 101.6, 57.2 , 47.7, 26.9, 20.9; IR (KBr) 3328, 2203, 1715, 1674, 1606, 1492, 1358 cm −1 ; FAB-HRMS m / z [M + H] + calcd for C 22 H 16 N 3 O 4 : 386.1141. Found: 386.1143.
Example 28 Preparation of Compound 49
5-methylisatin (6; 161 mg, 1.0 mmol), malononitrile (2; 66 mg, 1.0 mmol) in water (10 ml), and 4-hydroxy-6-methylcoumarin (43; 176 mg, 1.0 mmol) was reacted at 60 ° C. for 1 hour to obtain a solid compound 49 (338 mg, 88%).
mp> 300 ° C .; 1 H NMR (300 MHz, DMSO- d 6 ) δ 10.52 (1H, s, -NH), 7.75 (1H, s), 7.62-7.58 (4H, m), 7.04-6.96 (2H, m), 6.74- 6.72 (1 H, m), 2.44 (3 H, s), 2.19 (3 H, s); 13 C NMR (75 MHz, DMSO- d 6 ) δ 177.6, 166.0, 158.8, 155.4, 152.0, 150.6, 140.1, 134.8, 133.9, 131.4, 129.6, 125.0, 123.1, 122.6, 116.8, 112.6, 109.7, 101.9, 57.7 , 48.1, 21.0, 20.9 IR (KBr) 3359, 2199, 1708, 1672, 1498, 1358, 1212 cm −1 ; FAB-HRMS m / z [M + H] + calcd for C 22 H 16 N 3 O 4 : 386.1141. Found: 386.1143.
Example 29 Preparation of Compound 50
5-bromoissatin (7; 226 mg, 1.0 mmol), malononitrile (2; 66 mg, 1.0 mmol), and 4-hydroxy-6-methylcoumarin (43; 176 mg, in water (10 ml) 1.0 mmol) was reacted at 60 ° C. for 1 hour to obtain a solid compound 50 (395 mg, 88%).
mp> 300 ° C .; 1 H NMR (300 MHz, DMSO- d 6 ) δ 10.77 (1H, s, -NH), 7.75 (1H, s), 7.67 (2H, s), 7.60-7.58 (1H, m), 7.51 (1H, s), 7.40-7.38 (2H, m), 6.83-6.80 (1H, d, J = 8.4 Hz), 2.45 (3H, s); 13 C NMR (75 MHz, DMSO- d 6 ) δ 177.9, 159.6, 156.4, 151.3, 142.5, 136.4, 135.4, 132.6, 128.1, 123.2, 117.9, 117.4, 114.8, 113.3, 112.3, 101.7, 57.6, 49.8, 21.5 ; IR (KBr) 3359, 2199, 1708, 1672, 1498, 1358, 1212 cm −1 ; FAB-HRMS m / z [M + H] + calcd for C 21 H 13 BrN 3 O 4 : 450.0089. Found: 450.0086.
Claims (4)
[Formula 1]
(2)
(3)
In Chemical Formulas 1 to 3, the R, R 1 And R 2 is hydrogen, halogen or alkyl, R 3 is hydrogen, alkyl, phenyl, said R 4 and R 5 are hydrogen or alkyl and n is an integer from 0 to 1.
Preparing a mixture of isatin, malononitrile and 1,3-dicarbonyl compound in water;
Adding ethylenediamine diacetate to the mixture;
Stirring the reaction mixture at a temperature of 50 to 70 ° C. for 1 to 4 hours and then cooling to room temperature; And
A method for synthesizing a spirooxyindole derivative comprising the step of filtering, washing and drying the obtained material.
Preparing a mixture of 0.1-10 mmol of isatin, 0.1-10 mmol of malononitrile, and 0.1-10 mmol of 1,3-dicarbonyl compound in 5 ml of water;
Adding 0.01 to 1 mmol of ethylenediamine diacetate to the mixture at room temperature;
Stirring the reaction mixture at a temperature of 50 to 70 ° C. for 1 to 4 hours and then cooling to room temperature; And filtering, washing and drying the obtained material.
Synthesis method of spiroxyoxyindole derivative comprising a.
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