926219-14-9

Upstream product

• 1092075-57-4 2-amino-N-(tert-butyl)-N-[(5-methyl-2-furyl)methyl]-4,5-dimethoxybenzamide 
• 212780-02-4 3,4-dimethoxy-2-nitrobenzoic acid chloride 
• 349411-67-2 C₁₃H₁₈N₂O₅ 
• 5653-40-7 2-Amino-4,5-dimethoxybenzoic acid 
• 75-64-9 tert-butylamine 

Downstream Products

• 1427330-29-7 C₂₀H₂₅N₂O₃PS₂ 

Relevant academic research and scientific papers

Quinazoline dione derivatives and preparation method and application thereof

The invention provides novel quinazoline dione derivatives and a preparation method and application thereof. The compounds include compounds with the structure shown in the general formula V in the description and pharmaceutically acceptable salts or hydrates thereof. The compounds are active ligands of novel cannabinoid II receptors (CB2) and can be used for preparing medicine for treating, preventing and relieving CB2 receptor-mediated diseases, wherein the medicine is an agonist or partial agonist or inverse agonist or antagonist of CB2 receptors.

Reaction of vicinal thieno[2,3-b]pyridine aminoamides with Lawesson's reagent

The reaction of vicinal thieno[2,3-b]pyridine aminoamides with Lawesson's reagent gave new condensed diazaphosphinine derivatives. The structure of the substituent at the amide nitrogen atom and the reagent ratio were found to affect the direction of this

Some transformations of tertiary N-furfurylamides of aromatic and heteroaromatic carboxylic acids under acidic conditions

Acid-catalyzed transformations of tertiary N-furfurylamides of ortho-amino substituted aromatic and heteroaromatic carboxylic acids accompanied by elimination of the furfuryl moiety are investigated. Georg Thieme Verlag Stuttgart.