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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2065825Generated: October 31, 2026

tert-Butyl piperazine-1-carboxylate → tert-Butyl 4-(2-isocyanoacetyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/2065825

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantMethyl isocyanoacetateHCID 547815—
Producttert-Butyl 4-(2-isocyanoacetyl)piperazine-1-carboxylateHCID 86626953—

Reaction Steps

Prepared in accordance with Method B with methyl isocyanoacetate (2.51 g, 25.29 mmol) and piperazine-1-carboxylic acid tert-butyl ester (6.28 g, 33.85 mmol. The reaction mixture was stirred 1 h at RT and then concentrated. The residue was dissolved in dichloromethane (50 mL) and the organic layer was washed with 10% aqueous citric acid (2×25 mL), dried over MgSO4, filtered and evaporated. tert-Butyl 4-(2-isocyanoacetyl)piperazine-1-carboxylate SLA 07116C was obtained as a colorless oil (0.41 g, 6.5% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08288556B2
Source datasetuspto-grants-2012_10
ORD IDord-8ce722d7f05f4a0e8158255a82de1c0f
Source noteuspto-grants-2012_10