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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl 4-((4-aminophenyl)methyl)piperazine-1-carboxylate | HCID 12045001 | — |
| Reactant | 5-Pyrimidinecarboxylic acid, 2,4-dichloro-6-methyl-, ethyl ester | HCID 21517934 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 86677021 | HCID 86677021 | 61.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08729079B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-17963f407eab43f8a0b102386b0edbac |
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| Source note | uspto-grants-2014_05 |
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