24463-25-0

Basic information

• Product Name: 2(1H)-Quinoxalinone, 6-broMo-3,4-dihydro-3-Methyl-
• Synonyms: 2(1H)-Quinoxalinone, 6-broMo-3,4-dihydro-3-Methyl-;6-BroMo-3-Methyl-3,4-dihydroquinoxalin-2(1H)-one
• CAS NO: 24463-25-0
• Molecular Formula: C₉H₉BrN₂O
• Molecular Weight: 241.08456
• Mol File: 24463-25-0.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 392.4±42.0 °C(Predicted)
• Appearance: /
• Density: 1.497±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 12.93±0.40(Predicted)
• CAS DataBase Reference: 2(1H)-Quinoxalinone, 6-broMo-3,4-dihydro-3-Methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2(1H)-Quinoxalinone, 6-broMo-3,4-dihydro-3-Methyl-(24463-25-0)
• EPA Substance Registry System: 2(1H)-Quinoxalinone, 6-broMo-3,4-dihydro-3-Methyl-(24463-25-0)

Safety Data

• Hazardous Substances Data: 24463-25-0(Hazardous Substances Data)

Usage

Structure

Quinoxalinone derivative

Bromination

at position 6

Methylation

at positions 3 and 4

Potential pharmaceutical applications

Antipsychotic agent

Other potential properties

Antifungal and antimicrobial

Need for further research

Pharmacological and biological activities not yet fully understood

Upstream product

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Downstream Products

• 1417408-91-3 7-bromo-1-(2-chlorophenyl)-4-methyl-[1,2,4]triazolo[4,3-a]quinoxaline 
• 1427029-40-0 1-(2-chlorophenyl)-7-ethynyl-4-methyl-[1,2,4]triazolo[4,3-a]quinoxaline 
• 1427029-41-1 1-(2-chlorophenyl)-4-methyl-7-trimethylsilanylethynyl-[1,2,4]triazolo[4,3-a]quinoxaline 

Relevant articles and documents

DIHYDROQUINOXALINE BROMODOMAIN RECOGNITION PROTEIN INHIBITOR, PREPARATION METHOD AND USE THEREOF

The present invention relates to dihydroquinoxaline bromodomain recognition protein inhibitor, preparation method and use thereof. The inhibitor of the present invention is compound represented by general formula (I), or stereoisomer, pharmaceutically acceptable salt, prodrug, solvate, hydrate and crystal form thereof. The definition of each substituent is as described in the description and claims. The compound represented by general formula (I) of the present invention may inhibit bromodomain recognition protein and may be used for preparing medicament which regulates the apparent state of cells and treats series of diseases and symptoms which are mediated by the bromodomain recognition protein.

Synthesis of substituted 1,3-dimethyl-1H-quinoxalin-2-ones from aniline derivatives

Substituted 1,3-dimethyl-1H-quinoxalin-2-ones (7) have been synthesized through the procedures of acylation, nitration, reduction, intramolecular alkylation, oxidation, and N-methylation starting from 3,4-disubstituted aniline.

Benzimidazolones and analogues

The present invention provides compounds and pharmaceutical formulations useful as progesterone receptor agonists and antagonists and having the general formula: wherein: A is O, S, or NR4; B is a bond between A and C═Q, or the moiety CR5R6; R4, R5, R5are independently selected from H or optionally substituted C1to C6alkyl, C2to C6alkenyl, C2to C6alknyl, C3to C8cycloalkyl, substituted C3to C8cycloalkyl, aryl, or heterocyclic groups, or cyclic alkyl constructed by fusing R4and R5to from a 5 to 7 membered ring; R1is selected from H, OH, NH2, C1to C6alkyl, substituted C1to C6alkyl, C3to C6alkenyl, substituted C1to C6alkenyl, alkynyl, substituted alknyl, —COH, or optionally substituted —CO(C1to C3alkyl), —CO(aryl), —CO(C1to C3alkoxy), or —CO(C1to C3aminoalkyl) groups; R2is selected from H, halogen, CN, NO2, or optionally substituted C1to C6alkyl, C1to C6alkoxy, or C1to C6aminoalkyl groups; R3is selected from a trisubstituted benzene ring; or a 5- or 6-membered heteroaromatic ring containing 1 or 2 substituents; Q is O, S, NR8, or CR9R10; or a pharmaceutically acceptable salt thereof. The invention also includes methods of contraception and methods of treating or preventing maladies associated with the progesterone receptor.