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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 624537Generated: October 31, 2026

Triethylamine → tert-Butyl 3-(aminomethyl)-4-methylpiperazine-1-carboxylate

https://huagongshe.com/reaction/624537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantHCID 84689957HCID 84689957—
CatalystNickelHCID 935—
SolventMethanolHCID 887—
Producttert-Butyl 3-(aminomethyl)-4-methylpiperazine-1-carboxylateHCID 77474534—

Reaction Steps

To a solution of tert-butyl 3-cyano-4-methylpiperazine-1-carboxylate, prepared as described in Step A, (10.5 g, 47 mmol) in methanol (200 mL) was added metallic nickel (10 g) and triethylamine (5 mL). The mixture was stirred at ambient temperature overnight under atmosphere of hydrogen gas (50 psi). Upon consumption of tert-butyl 3-cyano-4-methylpiperazine-1-carboxylate, the mixture was filtered, and the filtrate was concentrated under vacuum to provide crude tert-butyl 3-(aminomethyl)-4-methylpiperazine-1-carboxylate used in the next step without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09303041B2
Source datasetuspto-grants-2016_04
ORD IDord-442f2223a8604285bf2b96bd8c52ea07
Source noteuspto-grants-2016_04