[1] GAO H,WANG Y,CHEN C,et al. Incorporation of lapatinib into core-shell nanoparticles improves both the solubility and anti-glioma effects of the drug[J]. Int. J. Pharm.,2014,461:478-488.
[2] HIGA G,ABRAHAM J. Lapatinib in the treatment of breast cancer[J]. Expert Rev. Anticancer Ther.,2007,7(9):1183-1192.
[3] 于丁,廖宁. 拉帕替尼联合卡培他滨治疗HER2过表达晚期乳腺癌的疗效评价[J]. 循证医学,2008,8(3):140-142. YU D,LIAO N. The therapeutic effect evaluation of lapatinib plus capecitabine for HER2 positive advanced breast cancer[J]. J. Evid.-Based Med.,2008,8(3):140-142.
[4] GNIAZDOWSKA E,KOZMINSKI P,BANKOWSKI K,et al. Synthesis,physicochemical and biological evaluation of technetium-99m labeled lapatinib as a novel potential tumor imaging agent of Her-2 positive breast cancer[J]. Eur. J. Med. Chem.,2014,87:493-499.
[5] LYU A,FANG L,GOU S. Design and synthesis of lapatinib derivatives containing a branched side chain as HER1/HER2 targeting anti-tumor drug candidates[J]. Eur. J. Med. Chem.,2014, 87:631-642.
[6] FRANKLIN M,CAREY K,VAJDOS F,et al. Insights into ErbB signaling from the structure of the ErbB2-pertuzumab complex[J]. Cancer Cell,2004,5:317-328.
[7] PATRICK J,GOODIN S. Lapatinib:a dual inhibitor of human epidermal growth factor receptor tyrosine kinases[J]. Clin. Ther., 2008,30(8):1426-1447.
[8] WALLACE E,TOPOLOV G,ZHAO Q,et al. Cyanoguanidines and cyanoamidines as ERBB2/EGFR inhibitors:US20050101617A1[P]. 2005-05-12.
[9] CHEW W,CHEAL G,LUNETTA J. Preparation methods of substituted 3-cyanoquinolines and their intermediates:WO2006127207[P]. 2006-11-30.
[10] TANG P,FENG J,FENG F, et al. Preparation methods of quinazoline derivatives and their pharmaceutical uses:WO2009012647A1[P]. 2009-01-29.
[11] ZHANG C,DUMAS J,ZHU Q,et al. Novel heterocycles:WO2006023843A2[P]. 2006-03-02.
[12] RAHEEM M,WEERATUNGA G,ZETINA-ROCHA C,et al. Process for the preparation of lapatinib and its ditosylate salt:US8952154B2[P]. 2011-12-23.
[13] LIU L, YUAN T, LIU H, et al. Synthesis and biological evaluation of substituted 6-alkynyl-4-anilinoquinazoline derivativesas potent EGFR inhibitors[J]. Bioorg. Med. Chem. Lett., 2007:6373-6377.
[14] 任晓岚,汪鑫,李志裕,等. 表皮生长因子受体(EGFR)酪氨酸激酶抑制剂的研究进展[J]. 中国新药杂志,2005,14(7):821-826. REN X L,WANG X,LI Z Y,et al. Research progresses of epidermal growth factor receptor tyrosine kinase inhibitors[J]. Chin. J. New Drugs,2005,14(7):821-826.
[15] EDWARD H, WEN C, CHEN P, et al. δ-Substituted pyrrolotriazine compounds:WO2005/065266[P]. 2005-07-21.
[16] ZHANG X,RAGHAVAN S,IHNAT M,et al. The design, synthesis and biological evaluation of conformationally restricted 4-substituted-2,6-dimethylfuro[2,3-d] pyrimidines as multi-targeted receptor tyrosine kinase and microtubule inhibitors as potential antitumor agents[J]. Bioorg. Med. Chem.,2015,23:2408-2423.
[17] NIE W, SONG W,ZHANG W, et al. miR-1470 mediates lapatinib induced p27 upregulation by targeting c-jun[J]. J. Cell. Physiol.,2015,230(7):1630-1639.
[18] 李连连,张庆文. 3-氯-4-(3-氟苄氧基)苯胺的合成[J]. 中国现代应用药学,2011,28(3):245-246. LI L L, ZHANG Q W. Practical synthesis of 3-chloro-4-(3-fluorobenzyloxy)aniline[J]. Chin. J. Mod. Appl. Pharm.,2011,28(3):245-246.
[19] FRANCESCO F,ALFREDO P. Efficient process for the preparation of lapatinib and salts thereof by means of new intermediates:US9024023B2[P]. 2013-09-03.
[20] 王武伟,江珂,李飞,等. N-(3-氯-4-(3-氟苯甲氧基)苯基)-6-碘喹唑啉-4-胺盐酸盐的合成[J]. 化工中间体,2008,11:28-30. WANG W W, JIANG K, LI F, et al. Synthesis of N-(3-chloro-4-((3-fluorobenzyloxy)phenyl)-6-iodoquinazolin-4-amine hydrochloride[J]. Chem. Intermed.,2008,11:28-30.
[21] 蔡志强,石玉,袁静,等. N-{3-氯-4-[(3-氟苄基)氧基]苯基}-6-碘喹唑啉-4-胺的合成工艺改进[J]. 合成化学,2011,19(3):421-424. CAI Z Q,SHI Y,YUAN J,et al. Process improvement on the synthesis of N-{3-chloro-4-[(3-fluorobenzyl)oxy]phenyl}-6-iodoquinazolin-4-amine[J]. Chin. J. Synth. Chem.,2011,19(3):421-424.
[22] 袁建勇,郭卿,李雁武. 一种制备拉帕替尼的方法和中间体:201510593037. 4[P]. 2015-09-12. YUAN J Y,GUO Q,LI Y W. Method for preparing lapatinib and intermediate:201510593037. 4[P]. 2015-09-12.
[23] 汪志勇,万常峰,王晔. 拉帕替尼中间体及其类似物的制备方法:201110189054.3[P]. 2011-07-07. WANG Z Y,WAN C F,WANG Y. Preparation method of lapatinib intermediate and analogues thereof:201110189054.3[P]. 2011-07-07.
[24] 李飞,王武伟,季兴,等. 拉帕替尼合成中间体的制备工艺:200910033327.8[P]. 2009-06-18. LI F,WANG W W,JI X,et al. Process for preparing lapatinib synthetic intermediate:200910033327.8[P]. 2009-06-18.
[25] JYOTHI P,ADINHATLA K,VENKAIAH C. Novel process for the preparation of lapatinib and its pharmaceutically acceptable salts:US20110263852[P]. 2011-10-27.
[26] 贾玉才,卢俊金,郑彦军,等. 拉帕替尼中间体N-[3-氯-4-(3-氟苄氧基)苯氨基]-6-碘喹唑啉的合成新方法[J]. 陕西师范大学学报(自然科学版),2013,41(6):42-45. JIA Y C,LU J J,ZHENG Y J,et al. A new method for synthesis of N-[3-chloro-4-(3-fluorophenzyloxy)phenyl]-6-iodoquinazolin-4-amine[J]. J.Shaanxi Norm. Univ. (Nat. Sci. Ed.),2013,41(6):42-45.
[27] ELKAMHAWY A,FARAG A,VISWANATH A,et al. Targeting EGFR/HER2 tyrosine kinases with a new potent series of 6-substituted-4-anilinoquinazoline hybrids:Design, synthesis, kinase assay,cell-based assay,and molecular docking[J]. Bioorg. Med. Chem. Lett.,2015,25:5147-5154.
[28] MCCLURE M S,ROSCHANGAR F,HODSON S J,et al. A practical one-pot synthesis of 5-aryl-2-furaldehydes[J]. Synthesis, 2001(11):1681-1685.
[29] ISMAIL R,ISMAIL N,ABUSERII S,et al. Recent advances in 4-aminoquinazoline based scaffold derivatives targeting EGFR kinases as anticancer agents[J]. Future J. Pharm. Sci.,2016,8:337-339.
[30] LACKEY K,SPECTOR N,WOOD E,et al. Pharmaceutical combination for the treatment of cancer containing a 4-quinazolineamine and another anti-neoplastic agent:WO02056912[P]. 2002-07-25.
[31] ESTOK T,ZAKNOEN S,MANSFIELD R,et al. Combination the rapy for the treatment of cancer using COX-2 inhibitors and dual inhibitors of EGFR (ErbB1) and HER2(Erb-B2):WO2009042613[P]. 2009-04-02.
[32] CARTER M,COCKERILL G,GUNTRIP S, et al. Bicyclic heteroaromatic compounds as protein tyrosine kinase inhibitors:US6727256[P]. 2004-04-27.
[33] ERICKSON G,GUO J,MCCLURE M, et al. Synthesis of lapatinib via direct regioselective arylation of furfural[J]. Tetrahedron Lett.,2014,55:6007-6010.
[34] KANO H,LIDA Y. Process for preparing 2-(methylsulfonyl)-ethylamine:JP2002020365[P]. 2002-01-23.
[35] PETROV K,ZHANG Y,CARTER M,et al. Optimization and SAR for dual ErbB-1/ErbB-2 tyrosine kinase inhibition in the 6-furanylquinazoline series[J]. Bioorg. Med. Chem. Lett.,2006,16:4686-4691.
[36] HWANG C,TARLTON E,PISCOPIO A. Process for the reduction of cyano-substituted sulfones to aminoalkylene-substituted Sulfones:WO2001083432[P]. 2001-11-08.
[37] 王武伟. 拉帕替尼及其中间体的合成研究[D]. 南京:南京医科大学,2009. WANG W W. Study on the synthesis of lapatinib and its intermediates[D]. Nanjing:Nanjing Medical University,2009.
[38] 张立鹏,齐英超,李斌,等. 一种拉帕替尼中间体的制备方法:201210534897[P]. 2013-04-10. ZHANG L P,QI Y C,LI B,et al. Preparation method of lapatinib intermediate:201210534897[P]. 2013-04-10.
[39] ABRAHAM S,BHAGWAT S,CAMPBELL B,et al. Quinazoline derivatives as raf-kinae modulators and methods of use thereof:WO2009117080[P]. 2010-11-04.
[40] TUNG R. 4-Aminoquinazoline derivatives and methods of use thereof:WO2008024439[P]. 2008-02-28.
[41] TUNG R,Morgan A. 4-Aminoquinazoline derivatives and methods of use thereof:US2011053964[P]. 2011-03-03.
[42] MCCLURE M,OSTERHOUT M,ROSCHANGAR F, et al. Quinazoline ditosylate salt compounds:WO2002002552A1[P]. 2002-01-10.
[43] 季兴,王武伟,许贯虹,等. 拉帕替尼的合成[J]. 中国医药工业杂志,2009,40(11):801-804. JI X,WANG W W,XU G H,et al. Synthesis of lapatinib[J]. Chin. J. Pharmaceut.,2009,40(11):801-804.
[44] 张庆文,周后元,尤启冬. 拉帕替尼合成工艺研究[J]. 中国药科大学学报,2010,41(4):317-320. ZHANG Q W,ZHOU H Y,YOU Q D. Practical synthesis of lapatinib[J]. J. Chin. Pharmaceut. Univ.,2010,41(4):317-320.
[45] JYOTHI P,ADIBHATLA K,VENKAIAH C. A novel process for the preparation of lapatinib and its pharmaceutically acceptable salts:WO2010061400[P]. 2010-06-03.
[46] 周艳红,袁哲东,王胡博,等. 一种制备拉帕替尼的方法:104109152[P]. 2014-10-22. ZHOU Y H,YUAN Z D,WANG H B,et al. Method for preparing lapatinib:104109152[P]. 2014-10-22.
[47] CHEN Y,HENSCHKE J,LIU Y,et al. Process and intermediates for preparing lapatinib:WO2011116634[P]. 2011-09-29.
[48] 王晶翼, 林栋, 冷传新, 等. 拉帕替尼的制备方法:102295638B[P]. 2010-06-24. WANG J Y,LIN D,LENG C X,et al. Novel method for preparing lapatinib:102295638B[P]. 2010-06-24.
[49] 庄韦,岳邦毅,陈强. 一种二对甲苯磺酸拉帕替尼的合成方法:103159747 A[P]. 2013-06-19. ZHUANG W, YUE B Y, CHEN Q. Synthetic method of lapatinib:103159747 A[P]. 2013-06-19. |