Abstract
The development of a stereospecific synthesis of a IDO1-selective inhibitor is described. The synthetic strategy toward enabling early discovery efforts along with additional findings pertaining to process safety that limited scalability are outlined. A convergent approach that supported the synthesis of material suitable for early preclinical and/or good laboratory practice toxicology studies and avoided the formation of key high-energy intermediates is summarized.
| Original language | English |
|---|---|
| Pages (from-to) | 1178-1190 |
| Number of pages | 13 |
| Journal | Organic Process Research & Development |
| Volume | 23 |
| Issue number | 6 |
| Early online date | 28 May 2019 |
| DOIs | |
| Publication status | Published - 21 Jun 2019 |
| Externally published | Yes |
Keywords
- Ido1
- Benzocyclobutylamine
- Oxadiazole
- Process safety
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