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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765638Generated: October 30, 2026

Ammonia → Benzyl (3R)-piperidin-3-ylcarbamate

https://huagongshe.com/reaction/1765638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant(R)-2-(((Benzyloxy)carbonyl)amino)pentane-1,5-diyl dimethanesulfonateHCID 66524788—
SolventTetrahydrofuranHCID 8028—
ProductBenzyl (3R)-piperidin-3-ylcarbamateHCID 1514176—

Reaction Steps

Liquid ammonia (ca. 30 ml) was added to a solution of (2R)-2-{[(benzyloxy)carbonyl]amino}-5-[(methylsulfonyl)oxy]pentyl methanesulfonate (1 g) in THF (15 ml) at −78° C. in a bomb reaction vessel and then the resultant mixture was allowed to reach room temperature. After 46 h, the solution was concentrated under reduced pressure to give an off-white solid which was purified using SPE (silica, eluting with methanol, methanol:aqueous ammonia 95:5, 9:1) to give the title compound (0.587 g) as an off white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07226929B2
Source datasetuspto-grants-2007_06
ORD IDord-c8946dbec48d42fe9d9c188dca76e916
Source noteuspto-grants-2007_06