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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 226388Erstellt: 26. Oktober 2026

Diisopropylethylamine → HCID 86603696, Verbindung

https://huagongshe.com/reaction/226388

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt4-ChloropyrimidineHCID 642834—
Eduktethyl (2E)-3-{5-[(3R)-3-piperidinylamino]-2-pyrazinyl)acrylate dihydrochlorideHCID 86603669—
LösungsmittelDimethylformamideHCID 6228—
ProduktHCID 86603696HCID 8660369646,3%

Reaktionsschritte

To a solution of ethyl (2E)-3-{5-[(3R)-3-piperidinylamino]-2-pyrazinyl}acrylate dihydrochloride (300 mg, 0.86 mmol) in DMF (6 mL) were added diisopropylethylamine (366 mg, 2.84 mmol) and 6-chloropyrimidine (128 mg, 1.11 mmol) at ambient temperature and the mixture was stirred at ambient temperature for 18 hrs. The reaction mixture was evaporated in vacuo and the residue was partitioned between water and EtOAc. The organic layer was separated, washed water and brine, dried over magnesium sulfate, and evaporated in vacuo. The residue was purified by silica gel column chromatography (chloroform-MeOH=95-5/hexane-EtOAc=¼) to give ethyl (2E)-3-(5-{[(3R)-1-(2-pyrimidinyl)-3-piperidinyl]amino}-2-pyrazinyl)acrylate (141 mg, 46%) as an amorphous powder.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07557127B2
Quelldatensatzuspto-grants-2009_07
ORD IDord-f2032b5a5059435d879d47024eaa4deb
Quellennotizuspto-grants-2009_07