Details

Heterocyclic Chemistry in Drug Discovery


Heterocyclic Chemistry in Drug Discovery


1. Aufl.

von: Jie Jack Li

123,99 €

Verlag: Wiley
Format: EPUB
Veröffentl.: 26.04.2013
ISBN/EAN: 9781118354438
Sprache: englisch
Anzahl Seiten: 720

DRM-geschütztes eBook, Sie benötigen z.B. Adobe Digital Editions und eine Adobe ID zum Lesen.

Beschreibungen

Enables researchers to fully realize the potential to discover new pharmaceuticals among heterocyclic compounds Integrating heterocyclic chemistry and drug discovery, this innovative text enables readers to understand how and why these two fields go hand in hand in the effective practice of medicinal chemistry. Contributions from international leaders in the field review more than 100 years of findings, explaining their relevance to contemporary drug discovery practice. Moreover, these authors have provided plenty of practical guidance and tips based on their own academic and industrial laboratory experience, helping readers avoid common pitfalls. Heterocyclic Chemistry in Drug Discovery is ideal for readers who want to fully realize the almost limitless potential to discover new and effective pharmaceuticals among heterocyclic compounds, the largest and most varied family of organic compounds. The book features: Several case studies illustrating the role and application of 3, 4, 5, and 6+ heterocyclic ring systems in drug discovery Step-by-step descriptions of synthetic methods and practical techniques Examination of the physical properties for each heterocycle, including NMR data and quantum calculations Detailed explanations of the complexity and intricacies of reactivity and stability for each class of heterocycles Heterocyclic Chemistry in Drug Discovery is recommended as a textbook for organic and medicinal chemistry courses, particularly those emphasizing heterocyclic chemistry. The text also serves as a guide for medicinal and process chemists in the pharmaceutical industry, offering them new insights and new paths to explore for effective drug discovery.
Chapter 1 Introduction 1 1.1 Nomenclature of Heterocycles 1 1.2 Aromatic Heterocycles 4 1.3 Importance of Heterocycles in Life 5 1.4 Importance of Heterocycles in Drug Discovery 8 PART I FIVE-MEMBERED HETEROCYCLES WITH ONE HETEROATOM 17 Chapter 2 Pyrroles 18 2.1 Introduction 18 2.2 Reactivity 22 2.3 Construction of the Pyrrole Rings 34 2.4 Palladium Chemistry of Pyrroles 44 2.5 Possible Liabilities of Pyrrole-Containing Drugs 46 2.6 Problems 49 2.7 References 51 Chapter 3 Indoles 54 3.1 Introduction 54 3.2 Reactivity of the Indole Ring 58 3.3 Construction of the Indole Rings 64 3.4 Oxindole-Containing Drug Synthesis 88 3.5 Cross-coupling Reactions for Indoles 91 3.6 Azaindole 104 3.7 Possible Liabilities of Drugs Containing 3-Methylindole 109 3.8 Problems 111 3.9 References 113 Chapter 4 Furans, Benzofurans, Thiophenes, and Benzothiophenes 119 4.1 Introduction 119 4.2 Furans and Benzofuran 126 4.3 Thiophenes and Benzothiophenes 158 4.4 Possible Liabilities of Furan and Thiophene-Containing Drugs 185 4.5 Problems 187 4.6 References 191 PART II FIVE-MEMBERED HETEROCYCLES WITH TWO OR MORE HETEROATOMS 197 Chapter 5 Pyrazoles, Pyrazolones, and Indazoles 198 5.1 Introduction 198 viii 5.2 Reactivity of the Pyrazoles and Indazoles 202 5.3 Construction of the Pyrazole and Indazole Rings 206 5.4 Pyrazolone-containing Drugs 217 5.5 Indazole-containing Drugs 220 5.6 Problems 223 5.7 References 226 Chapter 6 Oxazoles, Benzoxazoles, and Isoxazoles 231 6.1 Introduction 231 6.2 Construction of the Heterocyclic Ring 235 6.3 Reactivity 244 6.4 Cross-Coupling Reactions 250 6.5 Selected Reactions of Isoxazoles 269 6.6 Possible Liabilities of Oxazole-Containing Drugs 270 6.6 Problems 271 6.7 References 278 Chapter 7 Thiazoles and Benzothiazoles 283 7.1 Introduction 283 7.2 Reactions of the Thiazole Ring 290 ix 7.3 Palladium Chemistry Undergone by Thiazoles and Benzothiazoles 300 7.4 Construction of the Thiazole Ring 307 7.5 Construction of the Benzothiazole Ring 315 7.6 Possible Liabilities of Drugs Containing Thiazoles and Benzothiazoles 321 7.7 Thiazoles and Benzothiazoles as Bioisosteres 323 7.8 Problems 325 7.9 References 328 Chapter 8 Imidazoles and Benzimidazoles 333 8.1 Introduction to Imidazole 333 8.2 Reactivity of the Imidazole Ring 335 8.3 Construction of the Imidazole Ring 341 8.3.1 Debus 342 8.4 Conversion of Imidazolines to Imidazoles 353 8.5 Possible Liabilities of Imidazole-Containing Drugs 353 8.6 Introduction to Benzimidazole 354 8.7 Synthesis of Benzimidazoles: Classical Approaches 357 8.8 Construction of the Benzimidazole Core Using Transition Metal- Mediated Approaches 361 8.9 Alternative Cyclization Approach toward Benzimidazoles: Process Route toward BYK405879 367 8.10 Problems 368 8.11 References 370 Chapter 9 Triazoles and Tetrazoles 373 9.1 Introduction 373 9.2 Reactivity of the Triazole and Tetrazole Ring 375 9.3 Construction of the Triazole Ring 384 9.4 Possible Liabilities of Triazole-Containing Drugs 392 9.5 Problems 393 9.6 References 394 PART III SIX-MEMBERED HETEROCYCLES WITH ONE HETEROATOM 397 Chapter 10 Pyridines 398 10.1 Introduction 398 10.2 Reactivity of the Pyridine Ring 404 10.3 Construction of the Pyridine Ring 425 10.4. Problems 457 10.5 References 459 Chapter 11 Quinolines and Isoquinolines 471 11.1 Introduction 471 11.2 Reactivity of the Quinoline and Isoquinoline Ring 474 11.3 Construction of Quinoline Core 492 11.4 Construction of Isoquinoline Core 513 11.5 Possible Liabilities of Drugs Containing Quinoline and Isoquinoline Ring 526 11.6 Problems 527 11.7 References 528 PART IV SIX-MEMBERED HETEROCYCLES WITH TWO HETEROATOMS 535 Chapter 12 Pyrazines and Quinoxalines 536 12.1 Introduction 536 12.2 Formation of Diazines 539 12.3 Reactivity of the Molecules 545 12.4 Coupling Reactions 553 12.5 Problems 562 12.6 References 565 Chapter 13 Pyrimidines 569 13.1 Introduction 569 13.2 Construction of the Pyrimidine Ring 573 13.3 Synthesis of Pyrimidine-Containing Drugs 590 13.4 Problems 608 13.5 References 611 Chapter 14 Quinazolines and Quinazolones 615 14.1 Introduction 615 14.2 Reactions of Quinazolines and Quinazolinones 618 14.3 Quinazoline and Quinazolinone Synthesis 625 14.4 Synthesis of Quinazoline- and Quinazolinone-Containing Drugs 636 14.5 Problems 641 14.6 References 644 Subject Index 647
“The book can also serve as a textbook for undergraduates and graduates, which is highlighted by the inclusion of interesting problem sets.” (Angew. Chem. Int. Ed, 1 February 2014) “In summary, both students and experts in the field would find useful information in this book.” (ChemMedChem, 1 January 2014) “[Li] has assembled a team of 20 contributing authors from academia and the industry to write this book, which … comes across as a successful fusion of heterocyclic chemistry and drug discovery, from which intending medicinal chemists will derive much benefit, or as Li puts it, a ‘jump-start’ on the competition!.” (Chemistry in Australia, 1 July 2013)
JIE JACK LI, PhD, is a chemist at Bristol-Myers Squibb Company. He has authored or edited several books published by Wiley, including Name Reactions in Heterocyclic Chemistry, Name Reactions for Functional Group Transformations, Name Reactions for Homologations (Part I and Part ll ), Name Reactions for Carbocyclic Ring Formations, Contemporary Drug Synthesis, The Art of Drug Synthesis, and Modern Drug Synthesis.
Enables researchers to fully realize the potential to discover new pharmaceuticals among heterocyclic compounds Integrating heterocyclic chemistry and drug discovery, this innovative text enables readers to understand how and why these two fields go hand in hand in the effective practice of medicinal chemistry. Contributions from international leaders in the field review more than 100 years of findings, explaining their relevance to contemporary drug discovery practice. Moreover, these authors have provided plenty of practical guidance and tips based on their own academic and industrial laboratory experience, helping readers avoid common pitfalls. Heterocyclic Chemistry in Drug Discovery is ideal for readers who want to fully realize the almost limitless potential to discover new and effective pharmaceuticals among heterocyclic compounds, the largest and most varied family of organic compounds. The book features: Several case studies illustrating the role and application of 3, 4, 5, and 6+ heterocyclic ring systems in drug discovery Step-by-step descriptions of synthetic methods and practical techniques Examination of the physical properties for each heterocycle, including NMR data and quantum calculations Detailed explanations of the complexity and intricacies of reactivity and stability for each class of heterocycles Heterocyclic Chemistry in Drug Discovery is recommended as a textbook for organic and medicinal chemistry courses, particularly those emphasizing heterocyclic chemistry. The text also serves as a guide for medicinal and process chemists in the pharmaceutical industry, offering them new insights and new paths to explore for effective drug discovery.

Diese Produkte könnten Sie auch interessieren:

Enzymatic and Chemical Synthesis of Nucleic Acid Derivatives
Enzymatic and Chemical Synthesis of Nucleic Acid Derivatives
von: Jesús Fernández Lucas, María-José Camarasa Rius
PDF ebook
124,99 €
Enzymatic and Chemical Synthesis of Nucleic Acid Derivatives
Enzymatic and Chemical Synthesis of Nucleic Acid Derivatives
von: Jesús Fernández Lucas, María-José Camarasa Rius
EPUB ebook
124,99 €
Polymer Waste Management
Polymer Waste Management
von: Johannes Karl Fink
PDF ebook
150,99 €