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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 502398Generated: October 27, 2026

4-Amino-1-Boc-piperidine → 4-[4-(1-Methoxycarbonyl-1-methyl-ethyl)-benzoylamino]-piperidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/502398

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Amino-1-Boc-piperidineHCID 1268291—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant4-(1-Methoxycarbonyl-1-methyl-ethyl)-benzoic acidHCID 25111211—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product4-[4-(1-Methoxycarbonyl-1-methyl-ethyl)-benzoylamino]-piperidine-1-carboxylic acid tert-butyl esterHCID 6845476687.9%

Reaction Steps

0.780 g (3.78 mMol) of 4-amino-piperidine-carboxylic acid tert-butyl ester was suspended in 10 mL of MeCl2 at rt under argon; then, 0.80 g (3.60 mmol) of 4-(1-methoxycarbonyl-1-methyl-ethyl)-benzoic acid, 0.845 g (1.20 eq.) of N-(3-dimethylaminopropyl)-N′-ethyl-carbodiimide hydrochloride and 0.583 g (1.30 eq.) of N,N-dimethyl-4-aminopyridine were added. The reaction mixture became a clear solution after stirring for 1 h at rt. After 5 hours, the solution was evaporated i.V. and the residue was purified by chromatography (silicagel, eluent:MeCl2) to yield 1.28 g of the title compound as colorless foam. MS: 405.3 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07772253B2
Source datasetuspto-grants-2010_08
ORD IDord-584451639b8e40d58773cd129e745c34
Source noteuspto-grants-2010_08