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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1016545Generated: October 25, 2026

Ethyl isocyanate → N-(1-Boc-piperidin-3-yl-methyl)-N-phenyl-N'-ethylurea

https://huagongshe.com/reaction/1016545

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl isocyanateHCID 8022—
ReactantN-(1-Boc-piperidin-3-ylmethyl)anilineHCID 12972131—
ProductN-(1-Boc-piperidin-3-yl-methyl)-N-phenyl-N'-ethylureaHCID 1297213295%

Reaction Steps

To a solution of N-(1-Boc-piperidin-3-ylmethyl)aniline 1 (102 mg, 0.35 mmol) in 1 mL of dry CH2Cl2was added ethyl isocyanate (95%, 35 μL, 1.2 eq.) at room temperature. After being shaken at room temperature for overnight, the reaction mixture was passed through an aminopropyl NH2 cartridge and washed with CH2Cl2. Removal of the CH2Cl2 afforded N-(1-Boc-piperidin-3-yl-methyl)-N-phenyl-N′-ethylurea (2) (120 mg, 95%). LRMS 285 (M-100)+ 261.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06476050B2
Source datasetuspto-grants-2002_11
ORD IDord-edf865da5b9a422baf18473828b938ac
Source noteuspto-grants-2002_11