CAS: 1660-93-1; 3,4,7,8-Tetramethyl-1,10-Phenanthroline

相似化合物

3002-81-1 3248-05-3 3002-78-6

上下游产品

3,4-dimethyl-[8]quinolylamine 4-hydroxy-3-methyl-2-butanone 1,2-diamino-benzene 3,4-dimethyl-8-nitro-quinoline E-1,3-Dimethyl-5-undec-2-enyloxy-benzene 1-(benzyloxy)-3,5-dimethylbenzene tris-{3,4,7,8-tetramethyl-1,10-phenanthroline}iron(II) sulfate 3]2+[Ru(3,4,7,8-tetramethylphenanthroline)3]2+

4-羟基-3-甲基-2-丁酮置于arsenic(V) Oxide,乙醇,硫酸,Tin(Ll) Chloride体系中,化学反应 2.0H,反应生成3,4,7,8-四甲基-1,10-菲罗啉
参考文献:Substituted 1,10-Phenanthrolines. Iii.1,2 Polymethyl Phenanthrolines Related To 3,4-Dimethyl-1,10-Phenanthroline
标题:Substituted 1,10-Phenanthrolines. Iii.1,2 Polymethyl Phenanthrolines Related To 3,4-Dimethyl-1,10-Phenanthroline
摘要:
Doi:10.1021/ja01173A085

专利信息

专利号:US-12240835-B2
优先权日:2018-09-18
标题:Substituted benzamides as intermediates in the synthesis of inhibitors of tyrosine kinase enzymatic activity
发明人：ROMERO F ANTHONY; KIRSCHBERG THORSTEN A; HALCOMB RANDALL; XU YINGZI
权利人:TERNS PHARMACEUTICALS INC
摘要:Provided herein are compounds, preferably compounds inhibiting tyrosine kinase enzymatic activity of a protein selected from Abelson protein (ABL1), Abelson-related protein (ABL2), or a chimeric protein BCR-ABL1, compositions thereof, and methods of their preparation, and methods of inhibiting tyrosine kinase enzymatic activity of a protein selected from Abelson protein (ABL1), Abelson-related protein (ABL2), or a chimeric protein BCR-ABL1, and methods for treating diseases wherein modulation of BCR-ABL1 activity prevents, inhibits, or ameliorates the pathology and/or symptomology of the disease. Intermediates such as compounds of Formula (S23), which are useful in the synthesis of compounds inhibiting tyrosine kinase enzymatic activity of a protein selected from Abelson protein (ABL1), Abelson-related protein (ABL2), or a chimeric protein BCR-ABL1, are also provided.

专利号:WO-2018109082-A1
优先权日:2016-12-15
标题 :Process and intermediate for the preparation of 1-(4-(2-((1-(3,4- difluorophenyl)-1h-pyrazol-3-yl)methoxy)ethyl)piperazin-1-yl)ethanone
发明人：ALMANSA ROSALES CARMEN; CAAMAÑO MOURE ANA MARÃ?A; ENJO BABÃ?O JUAN
权利人:ESTEVE LABOR DR
摘要:The present invention relates to a process for the preparation of 1-(4-(2-((1-(3,4-difluorophenyl)-1H-pyrazol-3-yl)methoxy)ethyl)piperazin-1-yl)ethanone and salts and solvates thereof and to the use of intermediates in the synthesis of these compounds. Also is provided a new intermediate compound.

专利号:WO-2023137518-A1
优先权日:2022-01-21
标题 :Platinum complexes
发明人：ALDRICH-WRIGHT JANICE; GORDON CHRISTOPHER; DEO KRISHANT M; KHOURY ALEEN; MCGHIE BRONDWYN; APUTEN ANGELICO; PLATTEN-MENTI MARIA; RASHID FATIN; JURISINEC ASHLEY; SOLIMAN SARAH
权利人:WESTERN SYDNEY UNIV
摘要:The present disclosure relates to platinum complexes, and in particular platinum(II) and platinum(IV) complexes. The present disclosure also relates to synthesis of the platinum complexes, and to intermediates for the synthesis of the platinum complexes. The present disclosure also relates to methods and use of the platinum complexes for treating cancer.

专利号:WO-2021083438-A1
优先权日:2019-10-30
标 题:Inhibitors of purine nucleoside phosphorylase - synthesis and use thereof for treatment of t-cell acute lymphoblastic leukemia and lymphoma
发明人：SKACEL JAN; JANEBA ZLATKO; MERTLIKOVA KAISEROVA HELENA
权利人:USTAV ORGANICKE CHEMIE A BIOCHEMIE AV CR V V I
摘要:The present invention relates to new compounds of general formula I, their synthesis, their pharmaceutically acceptable salts, and their use in treatment of T-cell acute lymphoblastic leukemia and lymphoma.

专利号:US-2022289684-A1
优先权日:2019-08-29
标 题:Benzimidazole substitution-based phenyl n-butyramide compound and preparation method therefor
发明人：SHEN JINGSHAN; SUN CHANGLIANG; ZHU FUQIANG; ZHANG JUNCHI; LI RUI
权利人:TOPHARMAN SHANGHAI CO LTD; SHANGHAI INST OF MATERIAMEDICA CHINESE ACADEMY OF SCIENCES; TOPHARMAN TANCHENG CO LTD
摘要:The present disclosure relates to a benzimidazole-substituted phenyl-n-butyramide-based compound and the preparation method thereof. The method of the present disclosure avoids nitration reaction and polyphosphoric acid cyclization reaction, and avoids the generation of a large amount of waste acid reaction solution from the source. The synthesis method embodied in the invention has the advantages of simplicity and high efficiency, mild conditions and few pollutants, etc., and is suitable to be developed as a green and sustainable production process.

专利号:EP-3567040-B1
优先权日:2013-06-24
标 题 :Method for the preparation of intermediates useful for the synthesis of [1,2,4]-triazolo[4,3-a]pyridines