## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
The Reaction of 4-Oxo-4H-[1]benzopyran-3-carbaldehyde with 1,2-Benzenediamine. X-Ray Structure Analysis of the Reaction Product
✍ Scribed by Grety Rihs; Ivo Sigg; Georges Hass; Tammo Winkler
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- German
- Weight
- 126 KB
- Volume
- 68
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
Base1 (26.VIII.85) The reaction product of 4-oxo-4H-[l]benzopyran-3-carbaldehyde and 1,2-benzenediamine is 1,8-dihydro-6,13-bis(2-hydroxybenzoyl)dibenzo[b,i]-l,4,8,1l-tetraazacyclotetradeca-4,6,11,13-tetraene (l), and its dehydrogenation product is 3-(2-benzimidazolyl)-4H-[l]benzopyran-4-one (2) as shown by X-ray structure analysis confirming our earlier report. ') Atomic coordinates and bond lengths for 1 and 2 are available from the Crystallographic Data Centre, Cambridge (UK).
📜 SIMILAR VOLUMES
## Abstract magnified image The title aldehyde **1** reacts smoothly with the enamine moiety of **2**‐aminochromone **2** to produce hitherto unreported 3‐(2‐hydroxybenzoyl)‐5__H__‐1‐benzopyrano[2,3‐__b__]pyridin‐5‐one (azaxanthone) **5**. This reaction has been extended for the synthesis of bisaz
## Abstract The title aldehyde 1 in the presence of ammonia gives the pyridine derivatives 9‐11 respectively with acetylacetone, diethyl malonate and ethyl cyanoacetate, and ethyl (or methyl)‐l‐benzopyrano[4,3‐__b__]pyri‐dine‐3‐carboxylate **22** (or **23**) with ethyl (or methyl) acetoacetate. Ace