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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1971306Generated: October 30, 2026

Ammonia → (2R,4R)-1-tert-butyl 2-methyl 4-(3-(4-cyanophenyl)ureido)piperidine-1,2-dicarboxylate

https://huagongshe.com/reaction/1971306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantTriethylamineHCID 8471—
Reactant4-Cyanophenyl isocyanateHCID 170380—
Reactant(2R,4R)-1-tert-butyl 2-methyl 4-aminopiperidine-1,2-dicarboxylateHCID 54209755—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
Product(2R,4R)-1-tert-butyl 2-methyl 4-(3-(4-cyanophenyl)ureido)piperidine-1,2-dicarboxylateHCID 5753909493.6%

Reaction Steps

4-isocyanatobenzonitrile (1.17 g, 8.13 mmol) was added to a solution of (2R,4R)-1-tert-butyl 2-methyl 4-aminopiperidine-1,2-dicarboxylate (2.0 g, 7.7 mmol) and NEt3 (1.3 mL, 9.3 mmol) in THF (30 mL), and the resulting solution was stirred at room temperature for 6 hours. 1M ammonia in methanol (5 mL) was added to reaction mixture to quench excess isocyanine. Water (100 mL) and ethyl acetate (200 mL) were added to the mixture. The organic layer was separated and dried over MgSO4 and concentrated to give a solid. Purification was done by Companion (ReadySep, 80 g, silica gel packed) with ethyl acetate/heptane from 40-70% to give the urea as a white solid 2.9 g (90%). LC-MS: 403.2, 401.3 (t=2.6 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431597B2
Source datasetuspto-grants-2013_04
ORD IDord-163c62e754a840b18e03e0c89bcee111
Source noteuspto-grants-2013_04