HuagongsheHuagongshe Chemistry Print Report · For research reference only
phenyl(1H-pyrrolo[2,3-c]pyridin-2-yl)methanone → tert-Butyl 3-[[[phenyl(1H-pyrrolo[2,3-c]pyridin-2-yl)methylene]amino]oxy]piperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | phenyl(1H-pyrrolo[2,3-c]pyridin-2-yl)methanone | HCID 57893467 | — |
| Reactant | Tert-butyl 3-(aminooxy)piperidine-1-carboxylate | HCID 68983062 | — |
| Product | tert-Butyl 3-[[[phenyl(1H-pyrrolo[2,3-c]pyridin-2-yl)methylene]amino]oxy]piperidine-1-carboxylate | HCID 136366047 | — |
Reaction Steps
tert-Butyl 3-[[[phenyl(1H-pyrrolo[2,3-c]pyridin-2-yl)methylene]amino]oxy]piperidine-1-carboxylate was prepared from phenyl(1H-pyrrolo[2,3-c]pyridin-2-yl)methanone (Example 35) and tert-butyl 3-(aminooxy)piperidine-1-carboxylate (Reference Example 11) following the procedure described for Example 104 (geometry of the oxime double bond undefined).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07608627B2 |
| Source dataset | uspto-grants-2009_10 |
| ORD ID | ord-4a4957f18c3847b5ba175f8c1528ea6f |
| Source note | uspto-grants-2009_10 |