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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1765632Generated: October 25, 2026

Benzoic Acid → tert-Butyl 3-(benzoylamino)piperidine-1-carboxylate

https://huagongshe.com/reaction/1765632

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoic AcidHCID 243—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1-BOC-3-AminopiperidineHCID 545809—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
Producttert-Butyl 3-(benzoylamino)piperidine-1-carboxylateHCID 2201703339.1%

Reaction Steps

A solution of benzoic acid (0.123 g) in DMF (5 ml) was treated with 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (0.231 g), HOBT (0.163 g) and triethylamine (0.56 ml) and stirred at room temperature for 1 h. A solution of 3-amino-1-N-Boc-piperidine (0.3 g) in DMF (1 ml) was then added and stirring continued for 18 h. The solution was concentrated under reduced pressure to give an oil which was partitioned between ethyl acetate and water. The separated organic extracts were washed with water, hydrochloric acid (2N), saturated sodium bicarbonate solution and brine, dried (over magnesium sulphate) and concentrated under reduced pressure to give the title compound (0.120 g) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07226929B2
Source datasetuspto-grants-2007_06
ORD IDord-b7c7d5c57fcf42109abf79a459c9fb32
Source noteuspto-grants-2007_06