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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2085466Generated: November 2, 2026

Ammonia → (S)-1-N-Boc-Piperidine-2-carboxamide

https://huagongshe.com/reaction/2085466

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant(2S)-1-((tert-butoxy)carbonyl)piperidine-2-carboxylic acidHCID 688617—
ReactantPyBOPHCID 2724699—
SolventDimethylformamideHCID 6228—
Product(S)-1-N-Boc-Piperidine-2-carboxamideHCID 275682195%

Reaction Steps

Anhydrous ammonia gas was bubbled through a solution of (S)-(−)-1-(tert-butoxycarbonyl)-2-piperidine carboxylic acid (500 mg, 2.18 mmol) in DMF (50 ml) for 15 minutes. PyBop (1.25 g, 2.40 mmol) was added. After 5 hours, solvent was evaporated under reduced pressure. A solution of the resultant residue in ethyl acetate was washed with 5% citric acid (50 ml×3), 1 N NaOH (50 ml×3), dried with MgSO4, filtered, and concentrated to give 450 mg of (S)-2-carbamoyl-piperidine-1-carboxylic acid tert-butyl ester as a clear oil in 95% yield, which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06720346B2
Source datasetuspto-grants-2004_04
ORD IDord-fdd276dbdb014263959dff5cc73405d8
Source noteuspto-grants-2004_04