Synthesis of 5-amino-3a,4-dicyano-2,3,3a,6a-tetrahydrofuro[2,3-b]pyrroles
✍ Scribed by I. V. Moiseeva; P. M. Lukin; O. E. Nasakin; V. N. Romanov; V. A. Tafeenko; A. Kh. Bulai; P. A. Sharbatyan
- Publisher
- Springer US
- Year
- 1992
- Tongue
- English
- Weight
- 71 KB
- Volume
- 28
- Category
- Article
- ISSN
- 0009-3122
No coin nor oath required. For personal study only.
✦ Synopsis
5- 2, C15H13CIN206). This compound had mp 188-190~ (from AcOH). PMR spectrum (CD3CN): 2.40 (3H, s, CH3), 6.76-7.86 (9H, m, C6H4 and C6H5), 8.90 ppm (1H, s, OH). The yield was 41%.
5-(o-Hydroxyphenyl)-2,3-dimethyl-l,2,4-oxadiazolium Perchiorate (IV, CIoHllCIN206). This compound had mp 257-258~ (from AcOH). PMR spectrum (CF3COOH): 2.57 (3H, s, CH3), 4.1 (3H, s, N--CH3), 6.58-7.83 ppm (4H, m, C6H4). The yield was 47%.
LITERATURE CITED
.
📜 SIMILAR VOLUMES
## Abstract Previously synthesized 2‐(3′‐chloro‐5′,6′‐dicyanopyrazin‐2′‐yl)cyclopentan‐1‐one **1**, obtained from the reaction of 2,3‐dichloro‐5,6‐dicyanopyrazine with 1‐pyrrolidino‐1‐cyclopentene, was further reacted with primary alkylamines to give mixtures of diastereomer of 5‐alkyl‐2,3‐dicyano‐
## 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