CN105503835A - Novel quinazoline derivative LU1510 as well as preparation method and application thereof - Google Patents
Novel quinazoline derivative LU1510 as well as preparation method and application thereof Download PDFInfo
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Abstract
The invention discloses a novel quinazoline derivative LU1510 as well as a preparation method thereof. The quinazoline derivative LU1510 is chemically named N-4-[(4-dimethylamino phenyl)methoxy]phenyl-7-methoxy-6-[(1-pyrrole-2-yl)hydroxyethyl]quinazoline-4-amine. The quinazoline derivative as well as pharmaceutically acceptable salts, solvates and hydrates thereof has excellent in-vitro and in-vivo anti-tumor activity for MCF-7, SK-BR-3, MDA-MB-468 and U-87MG and has brighter application prospect in preparation of anti-tumor drugs.
Description
Technical field
The invention belongs to biomedicine field, relate to a kind of novel quinazoline quinoline derivant LU1510 and its preparation method and application particularly.
Background technology
Malignant tumour is a kind of common disease and frequently-occurring disease of serious threat human health, and over nearly 20 years, China's tumor mortality rate rises 29.42%.In 35 to 59 years old in prime of life crowd, tumour has arranged and has occupied first of all kinds of cause of the death.Data show: China's tumor incidence is about 2,00/,100,000 people, more than annual new cases about 2,200,000 people, controlling more than patient about 6,000,000 people.The methods for the treatment of of tumour has operative treatment, radiotherapy and chemotherapy.At present, chemotherapy remains the Main Means of clinical treatment tumour.Seeking antitumor medicine is one of focus of new drug research.In the last few years, 4-amino-quinazoline compound, because having excellent biological activity, enjoyed the extensive concern of people, became the focus that biological educational circles and region of chemistry scholars study.They produce good restraining effect to EGF acceptor or pdgf receptor Tyrosylprotein kinase, show the effect with anti-lung cancer, cancer of the stomach, colorectal carcinoma, mammary cancer, carcinoma of gallbladder and prostate cancer etc., antibacterial, AntiHIV1 RT activity, anti-inflammatory, the effects such as treatment diabetes, as marketed drug such as Gefitinib, Tarceva, xylene monosulfonic acid lapatinibditosylates.Contriver finds, N-4-[(4-dimethylamino phenyl) methoxyl group] phenyl-7-methoxyl group-6-[(1-pyrroles-2-base) hydroxyethyl] quinazoline-4-amine has certain anti-tumor activity, and contriver proposes the invention relevant to the pharmacy acceptable salt of N-4-[(4-dimethylamino phenyl) methoxyl group] phenyl-7-methoxyl group-6-[(1-pyrroles-2-base) hydroxyethyl] quinazoline-4-amine or this compound, solvate or prodrug or steric isomer or tautomer or metabolite.
Summary of the invention
Goal of the invention: for solving problems of the prior art, the invention provides a kind of novel quinazoline quinoline derivant LU1510, its chemical name is N-4-[(4-dimethylamino phenyl) methoxyl group] phenyl-7-methoxyl group-6-[(1-pyrroles-2-base) hydroxyethyl] quinazoline-4-amine, its to MCF-7, SK-BR-3, MDA-MB-468, U-87MG tetra-strain tumor cell proliferation there is inhibit activities.
Technical scheme: for realizing above-mentioned technical purpose, the invention provides a kind of novel quinazoline quinoline derivant LU1510, its chemical name is N-4-[(4-dimethylamino phenyl) methoxyl group] phenyl-7-methoxyl group-6-[(1-pyrroles-2-base) hydroxyethyl] quinazoline-4-amine, and its structural formula is as follows:
Present invention further proposes the preparation method of above-mentioned novel quinazoline quinoline derivant LU1510, comprise the steps:
S1: under nitrogen protection, pyrroles is dissolved in tetrahydrofuran (THF), slowly EtMgBr diethyl ether solution is dripped under ice bath, stir 30 minutes ~ 2 hours, reaction solution 0 ~ 60 DEG C stirs 30 minutes ~ 2 hours, 0 ~ 60 DEG C adds methyl bromoacetate and stirs 30 minutes ~ 2 hours, generates compound (1), i.e. 2-(1-pyrroles-2-base) acetic ester;
S2: under nitrogen protection, is dissolved in tetrahydrofuran (THF) by compound (1), adds LiAlH while stirring under ice bath in batches
4more than 30 minutes, obtain reduzate compound (2), i.e. 2-(1-pyrroles-2-base) ethanol;
S3: under nitrogen protection, by compound (2) and the chloro-7-methoxyquinazoline hydrochloride of 4--6-alcohol, PPh
3be dissolved in tetrahydrofuran (THF), under ice bath, add DTAD while stirring in batches, react more than 6 hours, generate compound (3), i.e. the chloro-7-methoxyl group of 4--6-[2-(1-pyrroles-2-base) hydroxyethyl] quinazoline;
S4: 4-dimethylaminobenzaldehyde is dissolved in tetrahydrofuran (THF), 0 ~ 25 DEG C adds sodium borohydride in batches, stirring reaction 4 ~ 12 hours, generates compound (4), i.e. 4-dimethylamino phenylcarbinol;
S5: by compound (4), dissolves with DMF, adds NaH, 25 ~ 100 DEG C are stirred 1 ~ 6 hour, 0 ~ 25 DEG C adds the fluoro-4-oil of mirbane of 1-in batches and generates compound (5), i.e. N, N-dimethyl-4-(4-nitre phenyl methyl) aniline;
S6: compound (5) is dissolved in tetrahydrofuran (THF), adds Raney's nickel in batches, pass into hydrogen, 25 ~ 60 DEG C of stirring reactions 4 ~ 12 hours, generate compound (6), i.e. 4-[(4-dimethylamino) phenyl] anisidine;
S7: by compound (3) with n-Butanol soluble, add compound (6), 25 ~ 100 DEG C are stirred 1 ~ 6 hour, generate compound (7), i.e. N-4-[(4-dimethylamino phenyl) methoxyl group] phenyl-7-methoxyl group-6-[(1-pyrroles-2-base) hydroxyethyl] quinazoline-4-amine.
Preferably, in step S1, the concentration of EtMgBr diethyl ether solution is 3M, drip speed be 5 ~ 10ml/min, EtMgBr ether, methyl bromoacetate, tetrahydrofuran (THF), pyrroles amount ratio be 100 ~ 500mL:20 ~ 50g:250 ~ 1000ml:20 ~ 50g.
In step S2, LiAlH
4consumption be that every g of compound (1) adds 0.25 ~ 2g.
In step S3, described DTAD divides 3 ~ 6 batches to add, 2 ~ 4 hours/time, interval, wherein, and the chloro-7-methoxyquinazoline hydrochloride of 4--6-alcohol, PPh
3, DTAD, compound (2) mole dosage ratio be 1: 1: 1: 0.8 ~ 1.4.
In step S4, described sodium borohydride divides 3 ~ 6 batches to add, 2 ~ 4 hours/time, interval, and the mole dosage ratio of 4-dimethylaminobenzaldehyde, sodium borohydride is 1: 0.6 ~ 2.4.
In step S5, described NaH divides 3 ~ 6 batches to add, 20 ~ 40 minutes/time, interval, and the mole dosage ratio of the fluoro-4-oil of mirbane of NaH, 1-and compound (4) is 1: 0.5 ~ 1.5: 0.5 ~ 1.5.
In step S6, the consumption of Raney's nickel be every g of compound (5) 0.2 ~ 1.5.
In step S7, the mole dosage ratio of compound (3), compound (6) is 1: 0.8 ~ 1.2.
Present invention further proposes above-mentioned novel quinazoline quinoline derivant and prepare the application in antineoplastic agent.
The present invention proposes a kind of pharmaceutical composition simultaneously, and said composition comprises the compound described in the claims 1 and pharmaceutically acceptable carrier.
Closer, the present invention proposes above-claimed cpd, or above-mentioned pharmaceutical composition is preparing the purposes in medicament.
Meanwhile, the invention allows for the pharmacy acceptable salt of above-mentioned novel quinazoline quinoline derivant LU1510 or this compound, solvate or prodrug or steric isomer or tautomer or metabolite and prepare the application in antineoplastic agent.
Finally, the present invention proposes the pharmacy acceptable salt of above-mentioned novel quinazoline quinoline derivant LU1510 or this compound, solvate or prodrug or steric isomer or tautomer or metabolite and one or more anticancer agents and be combined in purposes for the preparation for the treatment of on the medicine of tumour.
Beneficial effect: the invention discloses a kind of novel quinazoline quinoline derivant LU1510, and adopt mtt assay to evaluate it to suppress MCF-7, SK-BR-3, MDA-MB-468, U-87MG tetra-strain proliferative activity o f tumor, calculate the IC suppressing these four kinds of tumor cell proliferations
50value, result shows that prepared novel quinazoline quinoline derivant LU1510 is inhibited to above-mentioned tumour cell, can be used for preparing anti-tumor agent.
Accompanying drawing explanation
Fig. 1 is the synthetic route chart of quinazoline derivant, wherein: i) methyl bromoacetate, EtM
gbr, THF; Ii) THF, LiAlH
4; Iii) the chloro-7-methoxyquinazoline hydrochloride of 4--6-alcohol, PPh
3, DTAD, THF; Iv) NaBH
4, THF; V) 1-fluoro-4-nitrobenzene, NaH, DMF, vi) Raney's nickel, THF, H
2, vii) and n-BuOH.
Embodiment
In order to set forth the present invention further, provide a series of embodiment below.These embodiments are illustrative completely, and they are only used for being specifically described the present invention, not should be understood to limitation of the present invention.
Embodiment 1 prepares 2-(1-pyrroles-2-base) acetic ester (compound 1).
500mL tetrahydrofuran (THF) is placed in four neck round-bottomed flasks of the nitrogen protection of 2000mL, adds 50g pyrroles.Slowly drip 266.8mL3MEtMgBr diethyl ether solution under ice bath and stir 30min, dripping speed is 5ml/min.Reaction solution stirred at ambient temperature 1 hour, drips 45.7g methyl bromoacetate under ice bath, reaction solution stirred at rt for another 1 hour.Add 500mLof1NHCl termination reaction.Reaction solution is extracted with ethyl acetate 3 times, combined ethyl acetate layer, and saturated sodium-chloride water solution washes 3 times.Separate the ethyl acetate layer of merging, in 250mL triangular flask, add anhydrous sodium sulfate drying 6 hours, filtration under diminished pressure.Filtrate reduced in volume is to dry, and obtaining 19g (productive rate 46%) compound 1 through column chromatography, is brown oil.
Embodiment 2 prepares 2-(1-pyrroles-2-base) ethanol (compound 2).
19g2-(1-pyrroles-2-base) acetic ester (compound 1) is dissolved in 200mL tetrahydrofuran (THF), is placed in four neck round-bottomed flasks of the nitrogen protection of 500mL, under ice bath, adds 5.6gLiAlH in batches
4, stir 30min.5.6mL water is added, 15%NaOH16.8mL, stirring at room temperature 10min, termination reaction in reaction solution.Anhydrous sodium sulfate drying is added 6 hours, filtration under diminished pressure in 250mL triangular flask.Filtrate reduced in volume is to dry, and obtaining 10g (productive rate 66%) compound 2 through column chromatography, is brown oil.
The compound 2 of preparation is carried out
1h-NMR standard, result is as follows:
1H-NMR：(300MHz，DMSO-d
6，ppm)：δ8.52(brs，1H)，6.73-6.71(m，1H)，6.19-6.14(m，1H)，6.01-6.00(m，1H)，3.87-3.83(t，J＝5.7Hz，2H)，2.88-2.84(t，J＝5.7Hz，2H)。
Embodiment 3 prepares the chloro-7-methoxyl group of 4--6-[2-(1-pyrroles-2-base) hydroxyethyl] quinazoline (compound 3).
By chloro-for 12.6g4-7-methoxyquinazoline hydrochloride-6-alcohol, 6g2-(1-pyrroles-2-base) ethanol (compound 2), 17.1gPPh
3be dissolved in 150mL tetrahydrofuran (THF), be placed in three neck round-bottomed flasks of 250mL nitrogen protection, under ice bath, (point 4 batches, often criticize interval 2h) adds 15gDTAD, stirred overnight at room temperature in batches.Reaction mixture suction filtration filtering solid residue, filtrate reduced in volume is to dry.The resistates obtained, with obtaining 8.8g (productive rate 54%) compound 3 through column chromatography, is colourless powder.
Embodiment 4 prepares 4-dimethylamino phenylcarbinol (compound 4).
By 10g4-dimethylaminobenzaldehyde, be dissolved in 100mL tetrahydrofuran (THF), be placed in 250mL three-necked flask, ice bath under stirring in batches (point 4 batches, often criticize interval 2h) add 4.6g sodium borohydride, stirred overnight at room temperature.Add 30mL methyl alcohol termination reaction.Reaction solution is evaporated to dry, and obtaining 8g (productive rate 79%) compound 4 through column chromatography, is pale yellowish oil.
Embodiment 5 prepares N, N-dimethyl-4-(4-nitre phenyl methyl) aniline (compound 5)
By 8g4-dimethylamino phenylcarbinol (compound 4), be placed in the three-necked flask of 250mL, add 70mLDMF and dissolve, under ice bath, (point 4 batches, often criticize interval 30min) adds 4gNaH, stirring at room temperature 1 hour in batches.(divide 4 batches, often criticize interval 2h) in batches under reaction solution ice bath and add the fluoro-4-oil of mirbane of 7.5g1-, stirred overnight at room temperature, add 300mL frozen water termination reaction.Extraction into ethyl acetate 3 times, merges organic layer, washs 3 times, separate organic layer, add anhydrous sodium sulfate drying 6 hours, filtration under diminished pressure in 250mL triangular flask with saturated nacl aqueous solution.Filtrate reduced in volume is to dry, and obtaining 11g (productive rate 76%) compound 5 through column chromatography, is yellow powder.
Embodiment 6 prepares 4-[(4-dimethylamino) phenyl] anisidine (compound 6)
By 11gN, N-dimethyl-4-(4-nitre phenyl methyl) aniline (compound 5), be dissolved in 120mL tetrahydrofuran (THF), be placed in 250mL round-bottomed flask, add 2g Raney's nickel (divide 4 batches, often criticize interval 2h) in batches, pass into hydrogen, stirred overnight at room temperature.Reaction solution filtration under diminished pressure, filtrate is concentrated into dry, and obtaining 8g (productive rate 82%) compound 6 through column chromatography, is colourless powder.
Embodiment 7 prepares 4-{4-[(7-methoxyl group)-6-(1-pyrroles-2-base) hydroxyethyl] quinazoline-4-base } aminophenyiamino Methyl.alpha.-toluate (compound 7)
By chloro-for 1.5g4-7-methoxyl group-6-[2-(1-pyrroles-2-base) hydroxyethyl] quinazoline (compound 3), 1.2g4-[(4-dimethylamino) phenyl] anisidine (compound 6), be dissolved in 30mL propyl carbinol, be placed in 100mL tri-neck round-bottomed flask, 60 DEG C of oil baths stir 1 hour.Ice bath is cooled to room temperature, and reaction solution adds the dilution of 100mL water, and with aqueous sodium carbonate adjustment pH to 9, extraction into ethyl acetate 3 times, merge organic layer, saturated sodium-chloride water solution washes 2 times.Organic layer adds anhydrous sodium sulfate drying 6 hours in 250mL triangular flask, filtration under diminished pressure.Filtrate reduced in volume is to dry, and obtaining 0.718g (productive rate 14%) compound 7 through column chromatography, is buff powder.
To preparation compound 7 carry out ESI-MS,
1h-NMR standard, result is as follows:
ESI-MS(m/z)：510[M+H]
+；
1H-NMR(300MHz，DMSO-d
6，ppm)：δ10.71(s，1H)，9.46(s，1H)，8.38(s，1H)，7.84(s，1H)，7.58-7.55(d，J＝8.7Hz，2H)，7.29-7.26(d，J＝8.4Hz，2H)，7.17(s，1H)，7.02-6.99(d，J＝8.7Hz，2H)，674-6.71(d，J＝8.4Hz，2H)，6.66(s，1H)，5.94(s，2H)，4.96(s，2H)，4.30-4.25(t，J＝7.4Hz，2H)，3.94(s，3H)，3.14-3.09(t，J＝7.2Hz，2H)，2.90(s，6H)。
The evaluation of experimental example 8 compound 7 anti-tumour cell proliferative activity.
(1) given the test agent:
Compound 7 of the present invention is all mixed with desired concn with the substratum containing 0.1%DMSO.
(2) cell strain:
MCF-7 (human breast cancer cell, ATCC:HTB-22), SK-BR-3 (human breast cancer cell, ATCC:HTB-30), U-87MG (human brain astrocytes's blastoma, ATCC:HTB-14), MDA-MB-468 (human breast cancer cell, ATCC:HTB-132) 4 strain tumour cell equal purchased from American standard type culture collection institute (ATCC).
(3) key instrument and material
Ultrapure water instrument: MILLIPOREDirect-Q3;
High-pressure sterilizing pot: HVE-50, Hirayama company;
Digital display thermostat water bath: HH-4, Guo Hua Electrical Appliances Co., Ltd;
Super clean bench: VS-1300-U clean bench, SuZhou Antai Air Tech Co., Ltd.;
Cell incubation case: HF151UVCO2 incubator, Shanghai power Shengong department;
Refrigerated centrifuge: Anting Scientific Instrument Factory, Shanghai
Microplate reader: ELx800, Biotek company
Oscillator plate: ZD-9556, Taicang science and education equipment factory;
96 porocyte culture plates, 25cm
2culturing bottle: CorningCostar company;
2mL cryopreservation tube: CorningCostar company;
(4) main agents
RPMI-1640 substratum: Gibco company;
DMEM substratum: Gibco company;
L-15 substratum: Gibco company;
MEM substratum: Gibco company;
PBS damping fluid: Gibco company;
Foetal calf serum: Gibco company;
0.25% trypsin solution: Hyclone company;
MTT (four tetrazolium bromides): Sigma company, is dissolved in PBS solution, makes the solution of 5mg/mL, uses after filtration sterilization, keep in Dark Place;
Zorubicin (ADR): Beijing Hua Feng United Technologies Corp..
DMSO: DMSO, Sigma company;
(5) test method
MCF-7 cell selects DMEM substratum, and U-87MG cell selects MEM substratum, and MDA-MB-468 cell selects L-15 substratum, and other cells select RPMI-1640 substratum.Foetal calf serum and 80UmL all containing 10% fire extinguishing in substratum
-1penicillin and 0.08mgmL
-1streptomycin sulphate.
By good for growth conditions, be in MCF-7, SK-BR-3, MDA-MB-468, U-87MG cell of logarithmic phase by 1 × 10
4the density of individual/mL is inoculated in 96 orifice plates, every hole 100 μ l.Be placed in 37 DEG C, 5%CO
2cultivating in incubator treats adherent in 12 hours.Dosing cell hole by the concentration gradient preset add to be measured, through the compound 7 being dissolved in substratum of sterilising treatment, every hole 200 μ l, blanc cell hole adds isopyknic substratum, compared with control cells hole adds the Zorubicin (ADR) that equal-volume is dissolved in substratum, parallel 6 holes by the concentration gradient preset.At 37 DEG C, 5%CO
2cultivate after 48 hours in incubator, every hole adds the MTT solution that 10 μ l concentration are 5mg/mL, continues to be placed in 37 DEG C, 5%CO
2cultivate 4 hours in incubator.Careful sucking-off supernatant liquor, every hole adds 150 μ lDMSO dissolve purple residues (first a ceremonial jade-ladle, used in libation), and Oscillating Flat makes precipitation all dissolve in 10 minutes, measures O.D. value (absorbancy), wavelength 570nm in microplate reader.
The inhibiting rate of the sample under each sample concentration to tumour cell is calculated according to formula " relative survival rate=(D pastille-D is blank)/(it is blank that D contrasts-D) × 100% ".
Test parallel repetition 3 times, with inhibiting rate, compound concentration is mapped, calculate the IC of the compounds of this invention 7
50(half effective inhibition concentration) value.Adopt Zorubicin (ADR) as positive control medicine simultaneously.
(6) experimental result
Table 1 compound 7LU1510 anti-tumour cell proliferative activity (IC
50± SD μM)
| Compound | MCF-7 | SK-BR-3 | U-87MG | MDA-MB-468 |
| ADR | 3.98±0.07 | 4.65±0.02 | 82.47±7.15 | 2.45±0.31 |
| Compound 7 | 54.69±3.79 | 23.73±4.03 | 59.35±5.77 | 10.26±1.08 |
As shown in table 1, give the test result of compound 7 anti-tumour cell proliferative activity, result shows that prepared novel quinazoline quinoline derivant is inhibited to above-mentioned tumour cell, can be used for preparing anti-tumor agent.
Claims (12)
1. a novel quinazoline quinoline derivant LU1510, its chemical name is N-4-[(4-dimethylamino phenyl) methoxyl group] phenyl-7-methoxyl group-6-[(1-pyrroles-2-base) hydroxyethyl] quinazoline-4-amine, and the pharmacy acceptable salt of this compound, solvate or prodrug or steric isomer or tautomer or metabolite.
2. the preparation method of novel quinazoline quinoline derivant LU1510 according to claim 1, is characterized in that, comprise the steps:
S1: under nitrogen protection, pyrroles is dissolved in tetrahydrofuran (THF), slowly EtMgBr diethyl ether solution is dripped under ice bath, stir 30 minutes ~ 2 hours, reaction solution 0 ~ 60 DEG C stirs 30 minutes ~ 2 hours, 0 ~ 60 DEG C adds methyl bromoacetate and stirs 30 minutes ~ 2 hours, generates compound (1), i.e. 2-(1-pyrroles-2-base) acetic ester;
S2: under nitrogen protection, is dissolved in tetrahydrofuran (THF) by compound (1), adds LiAlH while stirring under ice bath in batches
4, stir more than 30 minutes, obtain reduzate compound (2), be i.e. 2-(1-pyrroles-2-base) ethanol;
S3: under nitrogen protection, by compound (2) and the chloro-7-methoxyquinazoline hydrochloride of 4--6-alcohol, PPh
3be dissolved in tetrahydrofuran (THF), under ice bath, add DTAD while stirring in batches, react more than 6 hours, generate compound (3), i.e. the chloro-7-methoxyl group of 4--6-[2-(1-pyrroles-2-base) hydroxyethyl] quinazoline;
S4: 4-dimethylaminobenzaldehyde is dissolved in tetrahydrofuran (THF), 0 ~ 25 DEG C adds sodium borohydride in batches, stirring reaction 4 ~ 12 hours, generates compound (4), i.e. 4-dimethylamino phenylcarbinol;
S5: by compound (4), dissolves with DMF, adds NaH, 25 ~ 100 DEG C are stirred 1 ~ 6 hour, 0 ~ 25 DEG C adds the fluoro-4-oil of mirbane of 1-in batches and generates compound (5), i.e. N, N-dimethyl-4-(4-nitre phenyl methyl) aniline;
S6: compound (5) is dissolved in tetrahydrofuran (THF), adds Raney's nickel in batches, pass into hydrogen, 25 ~ 60 DEG C of stirring reactions 4 ~ 12 hours, generate compound (6), i.e. 4-[(4-dimethylamino) phenyl] anisidine;
S7: by compound (3) with n-Butanol soluble, add compound (6), 25 ~ 100 DEG C are stirred 1 ~ 6 hour, generate compound (7), i.e. N-4-[(4-dimethylamino phenyl) methoxyl group] phenyl-7-methoxyl group-6-[(1-pyrroles-2-base) hydroxyethyl] quinazoline-4-amine.
3. the preparation method of novel quinazoline quinoline derivant LU1510 according to claim 2, it is characterized in that, in step S1, the concentration of EtMgBr diethyl ether solution is 3M, drip speed be 5 ~ 10ml/min, EtMgBr ether, methyl bromoacetate, tetrahydrofuran (THF), pyrroles amount ratio be 100 ~ 500mL: 20 ~ 50g: 250 ~ 1000ml: 20 ~ 50g; In step S2, LiAlH
4consumption be that every g of compound (1) adds 0.25 ~ 2g.
4. the preparation method of novel quinazoline quinoline derivant LU1510 according to claim 2, is characterized in that, in step S3, described DTAD divides 3 ~ 6 batches to add, 2 ~ 4 hours/time, interval, wherein, and the chloro-7-methoxyquinazoline hydrochloride of 4--6-alcohol, PPh
3, DTAD, compound (2) mole dosage ratio be 1: 1: 1: 0.8 ~ 1.4.
5. the preparation method of novel quinazoline quinoline derivant LU1510 according to claim 2, it is characterized in that, in step S4, described sodium borohydride divides 3 ~ 6 batches to add, 2 ~ 4 hours/time, interval, the mole dosage ratio of 4-dimethylaminobenzaldehyde, sodium borohydride is 1: 0.6 ~ 2.4.
6. the preparation method of novel quinazoline quinoline derivant LU1510 according to claim 2, it is characterized in that, in step S5, described NaH divides 3 ~ 6 batches to add, 20 ~ 40 minutes/time, interval, the mole dosage ratio of the fluoro-4-oil of mirbane of NaH, 1-and compound (4) is 1: 0.5 ~ 1.5: 0.5 ~ 1.5.
7. the preparation method of novel quinazoline quinoline derivant LU1510 according to claim 2, is characterized in that, in step S6, the consumption of Raney's nickel is every g of compound (5) 0.2 ~ 1.5.
8. the preparation method of novel quinazoline quinoline derivant LU1510 according to claim 2, is characterized in that, in step S7, the mole dosage ratio of compound (3), compound (6) is 1: 0.8 ~ 1.2.
9. a pharmaceutical composition, comprises the compound described in the claims 1 and pharmaceutically acceptable carrier.
10. compound according to claim 1, or pharmaceutical composition according to claim 9 is preparing the purposes in medicament.
The pharmacy acceptable salt of 11. novel quinazoline quinoline derivant LU1510 according to claim 1 or this compound, solvate or prodrug or steric isomer or tautomer or metabolite are preparing the application in antineoplastic agent.
The pharmacy acceptable salt of 12. novel quinazoline quinoline derivant LU1510 according to claim 1 or this compound, solvate or prodrug or steric isomer or tautomer or metabolite and one or more anticancer agents are combined in the application for the preparation for the treatment of in the medicine of tumour.
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| US20090143399A1 (en) * | 2003-10-14 | 2009-06-04 | Arizona Board Of Regents On Behalf Of The University Of Arizona | Protein Kinase Inhibitors |
| CN1993349A (en) * | 2004-06-04 | 2007-07-04 | 阿斯利康(瑞典)有限公司 | Quinazoline derivatives as ERBB receptor tyrosine kinases |
| CN102532042A (en) * | 2010-12-30 | 2012-07-04 | 上海医药工业研究院 | Aryl urea compound as well as intermediate and application thereof |
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