89694-47-3

Usage

Uses

4-Chloro-3-methoxyphenylboronic acid

InChI:InChI=1/C7H8BClO3/c1-12-7-4-5(8(10)11)2-3-6(7)9/h2-4,10-11H,1H3

Upstream product

• 16817-43-9 5-Bromo-2-chloroanisole 
• 121-43-7 Trimethyl borate 
• 50638-47-6 4-bromo-2-chloro-1-methoxybenzene 
• 766-51-8 2-Chloroanisole 
• 7732-18-5 water 
• 73183-34-3 bis(pinacol)diborane 

Downstream Products

• 918811-05-9 (4-amino-benzyl)-carbamic acid tert-butyl ester 
• 1338344-93-6 2-{2-[4-chloro-3-(methyloxy)phenyl]-1H-imidazol-4-yl}-N,N-dimethyl-1-[2-(methyloxy)ethyl]-1H-benzimidazole-5-carboxamide 
• 1338344-94-7 2-[2-(4-chloro-3-hydroxyphenyl)-1H-imidazol-4-yl]-N,N-dimethyl-1-[2-(methyloxy)ethyl]-1H-benzimidazole-5-carboxamide 
• 1338346-38-5 2-[2-[4-chloro-3-(methyloxy)phenyl]-1-({[2-(trimethylsilyl)ethyl]oxy}methyl)-1H-imidazol-4-yl]-N,N-dimethyl-1-[2-(methyloxy)ethyl]-1H-benzimidazole-5-carboxamide 
• 915201-06-8 (4-chloro-3-hydroxyphenyl)boronic acid 
• 18113-07-0 4-Chloro-3-methoxyphenol 

Relevant academic research and scientific papers

Regioselective Synthesis of o-Benzenediboronic Acids via Ir-Catalyzed o-C-H Borylation Directed by a Pyrazolylaniline-Modified Boronyl Group

Ir-catalyzed ortho-directed C-H borylation of pyrazolylaniline (PZA)-modified arylboronic acids with bis(pinacolate)diboron afforded o-benzenediboronic acids in which two boronyl groups are differentially modified by pinacol (PIN) and PZA. By using this borylation after nondirected Ir-catalyzed C-H borylation, o-benzenediboronic acids are conveniently synthesized from unfunctionalized arenes. The differentially modified o-benzenediboronic acids undergo selective oxidation and Suzuki-Miyaura cross-coupling at the PZA-modified boronyl groups, affording o-functionalized arylboronic acids selectively.

HETEROCYCLIC COMPOUNDS AND METHODS OF USE

The present application discloses compounds that are inhibitors of Btk, compounds that are inhibitors of ΡΒΚδ, and compounds that are dual inhibitors of both Btk and PI3Kδ. Also described are methods for synthesizing such inhibitors and methods for using such inhibitors for the treatment of diseases wherein inhibition of Btk and PI3Kδ provides a therapeutic benefit to a patient having the disease.

KYNURENINE-3-MONOOXYGENASE INHIBITORS, PHARMACEUTICAL COMPOSITIONS, AND METHODS OF USE THEREOF

Certain chemical entities are provided herein. Also provided are pharmaceutical compositions comprising at least one chemical entity and one or more pharmaceutically acceptable vehicle. Methods of treating patients suffering from certain diseases and diso

2-PYRIDONE COMPOUNDS

A 2-pyridone compound represented by the formula [1]: {wherein in the formula [1], the ring represented by A represents a benzene ring or a pyridine ring, X represents any of the structures represented by the formulas [3] shown below: V represents a single bond or a lower alkylene group, and W represents a single bond, an ether bond or a lower alkylene group (wherein the lower alkylene group may contain an ether bond)}, a tautomer or stereoisomer of the compound, a pharmaceutically acceptable salt thereof, or a solvate thereof is a compound that has an excellent GK activating effect and is useful as a pharmaceutical.

BENZAMIDE FACTOR VIIA INHIBITORS USEFUL AS ANTICOAGULANTS

The present invention provides novel benzamide derivatives of Formula (I): or a stereoisomer, tautomer, pharmaceutically acceptable salt, solvate, or prodrug thereof, wherein the variables A, W, Y, Z, R8, and R9 are as defined herein. These compounds are selective inhibitors of factor VIIa which can be used as medicaments.

Phenylglycinamide and pyridylglycinamide derivatives useful as anticoagulants

The present invention provides novel phenylglycinamide derivatives of Formula (I) or (IV): or a stereoisomer, tautomer, pharmaceutically acceptable salt, solvate, or prodrug thereof, wherein the variables W, W1, Y, Z, R7, R8, R9, and R11 are as defined herein. These compounds are selective inhibitors of factor VIIa which can be used as medicaments.

PHENYLGLYCINAMIDE DERIVATIVES USEFUL AS ANTICOAGULANTS

The present invention relates generally to phenylglycinamide derivatives that inhibit serine proteases. In particular it is directed to novel phenylglycinamide derivatives, and analogues thereof, which are useful as selective inhibitors of serine protease enzymes of the coagulation cascade; for example thrombin, factor VIIa, factor Xa, factor XIa, factor IXa, and/or plasma kallikrein. In particular, it relates to compounds that are factor VIIa inhibitors. This invention also relates to pharmaceutical compositions comprising these compounds and methods of using the same.