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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 416855Generated: October 30, 2026

tert-Butyl piperazine-1-carboxylate → Tert-butyl 4-(pyrimidin-5-ylmethyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/416855

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantPyrimidine-5-carboxaldehydeHCID 2761034—
ReactantSodium cyanoborohydrideHCID 5003444—
SolventAcetic AcidHCID 176—
SolventEthanolHCID 702—
ProductTert-butyl 4-(pyrimidin-5-ylmethyl)piperazine-1-carboxylateHCID 4686701755.1%

Reaction Steps

A solution of pyrimidine 5-carboxaldehyde (100 mg, 0.92 mmol) in ethanol (2 mL) and acetic acid (0.2 mL) at room temperature was treated with tert-butyl-1-piperazine carboxylate (2.5 eq, 2.31 mmol, 430 mg) and stirred for 5 minutes. Sodium cyanoborohydride (0.95 eq, 0.88 mmol, 55 mg) was added portionwise and the reaction then stirred for 16 h. Concentration in vacuo and preparative tlc purification (EtOAc) gave the product (141 mg, 55%) as a pale yellow oil; δH (500 MHz, CDCl3) 1.47 (s, 9H, C(CH3)3), 1.95 (br, 2H, piperazine NCH2), 2.42 (t, J=4.7 Hz, 2H, piperazine NCH2), 3.45 (t, J=4.9 Hz, 4H, piperazine N(CH2)2), 3.54 (s, 2H, CH2), 8.78 (s, 2H, pyrimidine H-4 & H-6), 9.15 (s, 1H, pyrimidine H-2);

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08088761B2
Source datasetuspto-grants-2012_01
ORD IDord-437bfc179a3e4385a3543f9da1740b65
Source noteuspto-grants-2012_01