HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 586468Generated: October 30, 2026
tert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylate → HCID 69206658, compound
https://huagongshe.com/reaction/586468
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylate | HCID 11737525 | — |
| Reactant | HCID 22329912 | HCID 22329912 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 69206658 | HCID 69206658 | 19.9% |
Reaction Steps
6-Benzyl-8-cyclopentyl-2-methanesulfinyl-8H-pyrido[2,3-d]pyrimidin-7-one (0.64 g, 1.74 mmol) and 4-(6-Amino-pyridin-3-yl)-piperazine-1-carboxylic acid tert-butyl ester (0.87 g, 2.96 mmol) in toluene (10 ml) were heated to 95° C. for 28 hours. The reaction mixture was allowed to cool then chromatographed on silica gel using a gradient of 20 to 50% ethyl acetate in hexane. The product-containing fractions were evaporated and the residue was triturated with acetonitrile to give a solid. This solid was collected by filtration and dried in vacuo to provide 4-[6-(6-benzyl-8-cyclopentyl-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidin-2-ylamino)-pyridin-3-yl]-piperazine-1-carboxylic acid tert-butyl ester (0.201 g, 19.8%). MS (APCI) M++1: Calc'd, 582.31. Found, 582.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06936612B2 |
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| Source dataset | uspto-grants-2005_08 |
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| ORD ID | ord-2d9c09bc015c44ad85a70278f6786f25 |
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| Source note | uspto-grants-2005_08 |
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