## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
Synthesis of 4,5-dichloro-1-(4,5-dichloropyridazin-3-yl)pyridazin-6-one
✍ Scribed by Deok-Heon Kweon; Young-Jin Kang; Hyun-A Chung; Jung-Won Park; Woo Song Lee; Yong-Jin Yoon; Sung-Kyu Kim; Motoo Shiro
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 1999
- Tongue
- English
- Weight
- 424 KB
- Volume
- 36
- Category
- Article
- ISSN
- 0022-152X
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract This paper presents the chlorination of 3,4,5‐trichloropyridazin‐6‐one and the synthesis of 3,4,5‐trichloro‐1‐(4,5,6‐trichloropyridazin‐3‐yl)pyridazin‐6‐one.
## Abstract Reaction of 1‐chloromethyl‐4,5‐dichloropyridazin‐6‐one with some nucleophiles such as sodium methoxide, sodium azide, 2‐mercaptopyrimidine and phenol gave 2, 3, 4, 7, 8 and 10. 5‐Chloro‐4‐phenoxypyridazin‐6‐one (10) was also synthesized from 8 through 9.
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a “Full Text” option. The original article is trackable v
## Abstract Direct functionalization of 4,5‐dichloropyridazin‐6‐one with some nucleophiles in seven solvents gave regioselectively 5‐halo‐4‐substituted‐pyridazin‐6‐ones as main product. Reaction of 4,5‐dichloropyridazin‐6‐one with 2‐mercaptopyrimidine (2 equivalents) also afforded 4,5‐di(pyrimidin‐