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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 272428Generated: October 31, 2026

HCID 11312463, compound → 4-[6-(8-Cyclopentyl-6-fluoro-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidin-2-ylamino)-pyridin-3-yl]-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/272428

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 11312463HCID 11312463—
Reactanttert-Butyl 4-(6-aminopyridin-3-yl)piperazine-1-carboxylateHCID 11737525—
SolventTolueneHCID 1140—
Product4-[6-(8-Cyclopentyl-6-fluoro-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidin-2-ylamino)-pyridin-3-yl]-piperazine-1-carboxylic acid tert-butyl esterHCID 1142082925.5%

Reaction Conditions

Temperature98 °C

Reaction Steps

8-Cyclopentyl-6-fluoro-2-methanesulfinyl-8H-pyrido[2,3-d]pyrimidin-7-one (2.0 g, 6.77 mmol, prepared accoring to Example 16) and 5 4-(6-Amino-pyridin-3-yl)-piperazine-1-carboxylic acid tert-butyl ester (6.0 g, 21 mmol) were added to toluene (8 ml) and heated to 98° C. for 18 hours. The mixture was filtered, washed with toluene and the solid suspended in diethyl ether. The mixture was filtered and the solid was dissolved in chloroform, washed with 1 N citric acid, brine and dried over anhydrous magnesium sulfate. The crude product was triturated with diethyl ether and dried in vacuo to provide 4-[6-(8-cyclopentyl-6-fluoro-7-oxo-7,8-dihydro-pyrido[2,3-d]pyrimidin-2-ylamino)-pyridin-3-yl]-piperazine-1-carboxylic acid tert-butyl ester as a solid (0.88 g, 25%). MS (APCI) M++1: Calc'd, 510.3. Found 510.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07456168B2
Source datasetuspto-grants-2008_11
ORD IDord-f87e3160868f4203a43449199ccff98f
Source noteuspto-grants-2008_11