97108-34-4Relevant academic research and scientific papers
Isolation of Anhydrous Hydrazine as Stable Inclusion Complexes with Hydroquinone and p-Methoxyphenol, and their Solid State Reaction with Esters which gives Pure Hydrazides
Toda, Fumio,Hyoda, Shunji,Okada, Kengo,Hirotsu, Ken
, p. 1531 - 1532 (1995)
Anhydrous hydrazine is isolated in a pure state as a stable inclusion complex crystal with hydroquinone or p-methoxyphenol, the X-ray structure of which have been analysed; the solid-state reaction of the hydrazine inclusion complex and esters gives hydrazides which are virtually uncontaminated with acid hydrazine salt byproducts.
Synthetic studies on compounds related to aminoimidazolecarboxamide: Synthesis of angularly fused purine derivatives and a solid phase ring transformation (ANRORC) to imidazo [1,5-a] pyrazine
Chattopadhyay, Gautam,Ray, Parlha Sinha
, p. 546 - 552 (2013/06/26)
l-Benzyl-5-aminoimidazole-4-carboxamide la has been used as a convenient precursor for the synthesis of new triazolo [3,4-i] purines 6 and the corresponding tetrazolo analogue 7. A mesoionic isomer 8 seems to exist along with 7. Interesting heteroaryl-purine motifs have also been prepared via suitably substituted 9-benzyIpurines. Imidazo |I,5-a| pyrazine derivative has been prepared in a solid phase exploitation of suitable imidazolium salt via ANRORC.
Hydrazine-hydroquinone complex as an efficient solid phase hydrazine donor: High yield synthesis of luminol and isoluminol
Chattopadhyay, Gautam,Ray, Partha Sinha
experimental part, p. 326 - 328 (2011/10/02)
Isomeric aminophthalhydrazides, luminol and isoluminol were easily obtained from the corresponding aminoph-thalimides by solid phase hydrazinolysis with the hydrazine-hydroquinone complex in high yields. Synthesis of a novel chemiluminescent agent, a heterocyclic analogue of isoluminol related to aminoimidazolecarboxamide, is also described.
