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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405060Generated: November 2, 2026

Ethyl Acetate → HCID 58513207, compound

https://huagongshe.com/reaction/1405060

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantSodium CarbonateHCID 10340—
Reactant4-(N-Boc-amino)piperidineHCID 723833—
ReactantHCID 58513427HCID 58513427—
SolventDimethyl SulfoxideHCID 679—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 58513207HCID 58513207—

Reaction Steps

The title compound is synthesized according to general procedure GP7 starting from 2.0 g (7.7 mmol) 4-chloro-6-methyl-5-(6-amino-pyridin-3-ylethynyl)-pyrimidin-2-ylamine and 1.7 g (8.47 mmol) piperidin-4-yl-carbamic acid tert-butyl ester using 1.07 ml (7.7 mmol) triethylamine in 3 mL NMP and 12 mL DMSO. 200 mL ethyl acetate and 100 mL half concentrated aqueous Na2CO3 solution are added and the phases are separated. The aqueous phase is extracted 2 times with ethyl acetate (100 mL each). The combined organic layers are dried over sodium sulfate and the solvent is removed under reduced pressure. The crude product is used without further purification in the next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916548B2
Source datasetuspto-grants-2014_12
ORD IDord-3e7e61b6bdd647c7b1c002ecbddcded5
Source noteuspto-grants-2014_12