HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272497Generated: October 31, 2026
tert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylate → HCID 11342019, compound
https://huagongshe.com/reaction/272497
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylate | HCID 11737525 | — |
| Reactant | HCID 22329913 | HCID 22329913 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 11342019 | HCID 11342019 | 20.4% |
Reaction Steps
8-Cyclopentyl-6-(2-ethoxy-ethyl)-2-methanesulfinyl-8H-pyrido[2,3-d]pyrimidin-7-one (1.0 g 2.86 mmol) and 4-(6-amino-pyridin-3-yl)-piperazine-1-carboxylic acid tert-butyl ester (1.10 g, 3.95 mmol) were heated to reflux in toluene (10 mL) for 16 hours. The mixture was cooled to room temperature and purified by silica gel chromatography to give 4-{6-[8-cyclopentyl-6-(2-ethoxy-ethyl)-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidin-2-ylamino]-pyridin-3-yl}-piperazine-1-carboxylic acid tert-butyl ester as an orange solid (0.328 g, 20.4%). 1H NMR δ(400 MHz, CDCl3) 8.54 (s, 1H), 8.26 (d, J=9.0 Hz, 1H), 7.98 (d, J=2.9 Hz, 1H), 7.45 (s, 1H), 7.38 (dd, J=2.9, 9.3 Hz, 1H), 5.90 (m, 1H), 3.70 (t, J=6.3, 1H), 3.61 (m, 4H), 3.51 (q, J=7.1, 1H), 3.11 (m, 4H), 2.84 (t, J=5.9, 1H), 2.33 (m, 2H), 2.08 (m, 2H), 1.87 (m, 2H), 1.69 (m, 2H), 1.48 (s, 9H), 1.19 (t, J=7.1, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07456168B2 |
|---|
| Source dataset | uspto-grants-2008_11 |
|---|
| ORD ID | ord-6f1cddcea1e74a4a86c4927262dac0fa |
|---|
| Source note | uspto-grants-2008_11 |
|---|