Abstract
A new and simplified method of preparing hexyloxy pyropheophorbide-a (HPPH), a promising agent used in photodynamic therapy, is described. This method is carried out in two processing steps, replacing an older method requiring five steps. This is accomplished by means of a Dieckmann condensation and subsequent thermal decarboxylation, both occurring in the same high-boiling solvent, thus reversing the long-standing trend in which naturally occurring chlorin derivatives with exocyclic rings are often subjected to conditions that open this ring to obtain chlorin derivatives. In the new process, a raw material without an exocyclic ring is used to construct a product containing the exocyclic ring. The new method does not require cryogenic processing or chromatography, removing the most significant obstacles to large-scale preparation of HPPH and its homologues.
| Original language | English |
|---|---|
| Pages (from-to) | 287-290 |
| Number of pages | 4 |
| Journal | Organic Process Research and Development |
| Volume | 8 |
| Issue number | 2 |
| DOIs | |
| State | Published - Mar 2004 |
Fingerprint
Dive into the research topics of 'Efficient synthesis of pyropheophorbide-a and its derivatives'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver