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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 408454Generated: October 31, 2026

(3R,4R)-benzyl 3-(tert-butoxycarbonylamino)-4-(methylsulfonyloxy)piperidine-1-carboxylate → HCID 58386792, compound

https://huagongshe.com/reaction/408454

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(3R,4R)-benzyl 3-(tert-butoxycarbonylamino)-4-(methylsulfonyloxy)piperidine-1-carboxylateHCID 58386823—
SolventPyridineHCID 1049—
ProductHCID 58386792HCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08759338B2
Source datasetuspto-grants-2014_06
ORD IDord-1474c3398a9542b092c6894e6fb77006
Source noteuspto-grants-2014_06