Nitrafudam

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Nitrafudam
Nitrafudam.svg
Identifiers
CAS Number
PubChem CID
ChemSpider
UNII
ChEMBL
Chemical and physical data
Formula C11H9N3O3
Molar mass 231.211 g·mol−1
3D model (JSmol)
  • C1=CC=C(C(=C1)C2=CC=C(O2)C(=N)N)[N+](=O)[O-]
  • InChI=1S/C11H9N3O3/c12-11(13)10-6-5-9(17-10)7-3-1-2-4-8(7)14(15)16/h1-6H,(H3,12,13)
  • Key:FYUZOMGBPKUZNJ-UHFFFAOYSA-N

Nitrafudam is an antidepressant compound that was developed in the 1970-1980s. [1] [2] It contains three functional groups: a nitrobenzene, a furan ring and an amidine.

Synthesis

Nitrafudam synthesis Nitrafudam synthesis.svg
Nitrafudam synthesis

Azo coupling between 2-nitrophenyldiazonium chloride [119-66-4] (1) and furfural (2) leads to 5-(2-nitrophenyl)furfural [20000-96-8] (3). Treatment of the aldehyde with hydroxylamine gives the corresponding aldoxime (PC789659). Upon dehydration, FGI to the nitrile occurs [57666-58-7] (4). A Pinner reaction with anhydrous methanolic hydrogen chloride gives the corresponding imidate (imino-ether) [62821-40-3] (5). An addition-elimination reaction with ammonia causes FGI to an amidine, thus completing the synthesis of nitrafudam (6).

References

  1. Pong SF, Pelosi SS, Wessels FL, Yu CN, Burns RH, White RE, et al. (1983). "5-phenyl-2-furamidines: a new chemical class of potential antidepressants". Arzneimittel-Forschung. 33 (10): 1411–1416. PMID   6140016.
  2. US 3919231,Pelosi SS Jr, White RE, White RL Jr, Wright GC, You CN,issued 1975, assigned to Morton Norwich Products Inc