61903-11-5

Usage

Chemical Properties

Clear colorless to light yellow liquid

InChI:InChI=1/C7H14N2O/c1-7(10)9-5-2-3-8-4-6-9/h8H,2-6H2,1H3

Upstream product

• 505-66-8 1,4-Diazacycloheptane 
• 108-24-7 acetic anhydride 

Downstream Products

• 864296-08-2 4-(4-N-acetyl-[1,4]diazepan-1-yl)-3-chloro-benzonitrile 
• 1160829-54-8 C₂₁H₂₂F₂N₄O 
• 1190058-01-5 N-(7-(4-acetyl-1,4-diazepan-1-yl)pyrazolo[1,5-a]pyrimidin-5-yl)-4-(2-hydroxypropan-2-yl)benzamide 
• 1190058-27-5 N-(7-(4-acetyl-1,4-diazepan-1-yl)-2-methylpyrazolo[1,5-a]pyrimidin-5-yl)-4-(2-hydroxypropan-2-yl)benzamide 
• 1190058-03-7 N-(7-(4-acetyl-1,4-diazepan-1-yl)-2-ethylpyrazolo[1,5-a]pyrimidin-5-yl)-4-(2-hydroxypropan-2-yl)benzamide 
• 1022258-79-2 1-[4-(4-fluorobenzenesulfonyl)-[1,4]diazepan-1-yl]ethanone 
• 1198794-91-0 1-(4-benzoyl[1,4]diazepan-1-yl)ethanone 
• 1198794-90-9 1-(4-acetyl-[1,4]diazepan-1-yl)-2-phenylethanone 
• 1179344-53-6 2-({2-[({3'-[(4-acetylhexahydro-1H-1,4-diazepin-1-yl)methyl]-6-fluoro-3-biphenylyl}methyl)amino]-2-oxoethyl}oxy)-N-{[1,6-diethyl-4-(tetrahydro-2H-pyran-4-ylamino)-1H-pyrazolo[3,4-b]pyridin-5-yl]methyl}acetamide 
• 1040718-40-8 5-(4-acetyl-[1,4]diazepan-1-yl)-N-(5-(4-methoxyphenyl)-1H-pyrazol-3-yl)pentanamide 
• 497249-20-4 C₁₄H₁₉N₃O₃ 
• 1042918-53-5 1-acetyl-4-(4-bromophenyl)-[1,4]diazepan 
• 1040724-82-0 5-[5-(4-acetyl[1,4]diazepan-1-yl)-2-methylpentanoylamino]-3-(4-methoxyphenyl)pyrazole-1-carboxylic acid tert-butyl ester 
• 3619-73-6 1-ethyl-1,4-homopiperazine 

Relevant academic research and scientific papers

Design, synthesis and nootropic activity of new analogues of sunifiram and sapunifiram, two potent cognition-enhancers

A series of amides and sulfonamides, structurally related to DM235 (sunifiram) and MN19 (sapunifram), derived by ring expansion or contraction, or by inversion of the exocyclic amide function, have been syn-thesized and tested for cognition-enhancing acti

Mono-acylation of piperazine and homopiperazine via ionic immobilization

A method for the selective mono-acylation of piperazine and homopiperazine has been developed. In a flow system, initially the diamine is ionically immobilized on a sulfonic acid funtionalized silica gel, acylated with an appropriate reagent and finally liberated with ammonic methanol. Examples with high yield and purity are presented.