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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1025377Generated: October 27, 2026

tert-Butyl 4-((4-aminophenyl)methyl)piperazine-1-carboxylate → HCID 86677021, compound

https://huagongshe.com/reaction/1025377

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-((4-aminophenyl)methyl)piperazine-1-carboxylateHCID 12045001—
Reactant5-Pyrimidinecarboxylic acid, 2,4-dichloro-6-methyl-, ethyl esterHCID 21517934—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 86677021HCID 8667702161.4%

Reaction Conditions

Temperature0 °C

Reaction Steps

Ethyl 2,4-dichloro-6-methylpyrimidine-5-carboxylate (0.5 g, 2.1 mmol) and tert-butyl 4-(4-aminobenzyl)piperazine-1-carboxylate (0.6 g, 2.06 mmol) were dissolved in NMP and stirred at 0° C. for 2 hour. The reaction mixture was poured onto water and extracted with EtOAc. The organic layer was washed with water, dried over Na2SO4 and evaporated under vacuum to get the desired compound (0.62 g). 1H NMR (400 MHz, CDCl3): δ 10.58 (s, 1H), 7.58 (d, J=6.4 Hz, 2H), 7.31 (d, J=6.4 Hz, 2H), 4.45 (q, J=6.8 Hz, 2H), 3.56 (s, 2H), 3.41 (m, 4H), 2.69 (s, 3H), 2.47 (m, 4H), 1.45 (s, 9H), 1.43 (t, J=6.8 Hz, 3H); MS m/z 490.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08729079B2
Source datasetuspto-grants-2014_05
ORD IDord-17963f407eab43f8a0b102386b0edbac
Source noteuspto-grants-2014_05