HuagongsheHuagongshe Chemistry Print Report · For research reference only
(3R,4R)-benzyl 3-(tert-butoxycarbonylamino)-4-(methylsulfonyloxy)piperidine-1-carboxylate → HCID 58386792, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (3R,4R)-benzyl 3-(tert-butoxycarbonylamino)-4-(methylsulfonyloxy)piperidine-1-carboxylate | HCID 58386823 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | HCID 58386792 | HCID 58386792 | — |
Reaction Steps
A solution of (3R,4R)-benzyl 3-(tert-butoxycarbonylamino)-4-(methylsulfonyloxy)piperidine-1-carboxylate in pyridine (0.16 M) was heated to 120° C. in the microwave for 10 minutes. The solution was then concentrated to almost dryness and the forming solid was filtered to give the desired product. The filtrate was further purified via silica gel column chromatography eluting with ethyl acetate (100%) to yield (3aR,7aS)-benzyl 2-oxohexahydrooxazolo[4,5-c]pyridine-5(6H)-carboxylate in 75% combined yield. LCMS (m/z): 277.1 (MH+), Rt=2.327 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08829193B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-bb3af80ba43c4abca78a9dd8a6dfdda7 |
| Source note | uspto-grants-2014_09 |