69585-93-9

Upstream product

• 2999-46-4 Ethyl isocyanoacetate 
• 814-49-3 diethyl chlorophosphate 
• 2886-65-9 7-chloro-5-(2-fluorophenyl)-1,3-dihydro-1,4-benzodiazepin-2(2H)-one 
• 784-38-3 2-amino-5-chloro-2'-fluorobenzophenone 
• 1584-62-9 2?(2?bromoacetamido)?5?chloro?2'?fluorobenzophenone 
• 59688-88-9 di-morpholin-4-yl-phosphinic acid 7-chloro-5-(2-fluoro-phenyl)-3H-benzo[e][1,4]diazepin-2-yl ester 

Downstream Products

• 59467-70-8 Midazolam 
• 59468-46-1 8?chloro-6?(2?fluorophenyl)?4H?imidazo[1,5?a][1,4]benzodiazepine?3?carboxylic acid 

Relevant academic research and scientific papers

Improved and scalable methods for the synthesis of midazolam drug and its analogues using isocyanide reagents

Abstract: In this research, two improved and scalable methods for the synthesis of midazolam and its analogues have been described. Midazolam has been synthesized using isocyanide reagents in satisfactory yield. In this methodology, imidazobenzodiazepine intermediates can be easily prepared via an improved process. One-pot condensation of benzodiazepines with mono-anion of tosylmethyl isocyanide or ethyl isocyanoacetate under mild condition led to formation of imidazobenzodiazepine. In the first method, tosylmethyl isocyanide (Tos-MIC) is used and the number of synthetic steps are decreased in comparison to previous report. In the second method, ethyl isocyanoacetate which is commonly used for the synthesis of some imidazobenzodiazepines, is consumed to generate midazolam. The latter, a relatively different method for the synthesis of midazolam analogues has been reported. Graphical abstract: [Figure not available: see fulltext.].

Synthesis of imidazo[1,5-a]diazepine-3-carboxylates

A process to produce diazepine-3-carboxylates of the formula STR1 is selected from the group consisting of STR2 R6 is selected from the group consisting of hydrogen, halogen, nitro, cyano, trifluoromethyl, lower alkyl, and lower alkanoyl; Rsub