Chemistry:Imolamine
From HandWiki
Short description: Chemical compound
![]() | |
![]() | |
Clinical data | |
---|---|
Trade names | Angolon, Angoril, Circuline, Irri-Cor, Irrigor, Coremax |
ATC code | |
Identifiers | |
| |
CAS Number | |
PubChem CID | |
DrugBank | |
ChemSpider | |
UNII | |
KEGG | |
ChEMBL | |
Chemical and physical data | |
Formula | C14H20N4O |
Molar mass | 260.341 g·mol−1 |
3D model (JSmol) | |
| |
| |
![]() ![]() |
Imolamine (INN, BAN; brand names Angolon, Angoril, Circuline, Irri-Cor, Irrigor, Coremax) is a coronary vasodilator which is used in the treatment of angina pectoris and as a local anesthetic.[1][2]
Synthesis
Butalamine has very similar synthesis but is alkylated on the alternate nitrogen position.
The reaction of benzoylchloride oxime [698-16-8] (2) with Cyanamide (3) gives 3-Phenyl-1,2,4-oxadiazol-5-amine [3663-37-4] (4). Alkylation with 2-chlorotriethylamine [100-35-6] (5) in the presence of KOH base occurs at the endocyclic ring nitrogen completing the synthesis of imolamine (6).
EFforts towards Onepot method (section 2.5 & 2.6).
References
- ↑ Index Nominum 2000: International Drug Directory. Taylor & Francis. January 2000. pp. 547–. ISBN 978-3-88763-075-1. https://books.google.com/books?id=5GpcTQD_L2oC&pg=PA547.
- ↑ The Dictionary of Drugs: Chemical Data: Chemical Data, Structures and Bibliographies. Springer. 14 November 2014. pp. 680–. ISBN 978-1-4757-2085-3. https://books.google.com/books?id=0vXTBwAAQBAJ&pg=PA680.
- ↑ Anne Rolland, EP patent 0191253 (1986 to Laboratoires Albert Rolland SA).
- ↑ Anne Rolland, FR patent 2576789 (1986 to Laboratoires Albert Rolland SA).
- ↑ FR2023M idem J M D Aron-Samuel & J J Sterne, GB patent 1010231 (1965-11-17).
![]() | Original source: https://en.wikipedia.org/wiki/Imolamine.
Read more |