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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272434Generated: October 31, 2026

tert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylate → HCID 69206658, compound

https://huagongshe.com/reaction/272434

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylateHCID 11737525—
ReactantHCID 22329912HCID 22329912—
SolventTolueneHCID 1140—
ProductHCID 69206658HCID 6920665819.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456168B2
Source datasetuspto-grants-2008_11
ORD IDord-b7c2e77c0dae46c2b763864bca66d044
Source noteuspto-grants-2008_11