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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 473593Erstellt: 25. Oktober 2026

3-Oxo-azetidine-1-carboxylic acid tert-butyl ester → 3-(3-Oxo-4-pyrimidin-2-yl-piperazin-1-yl)-azetidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/473593

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Oxo-azetidine-1-carboxylic acid tert-butyl esterHCID 1519404—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt3-Oxo-4-pyrimidin-2-yl-piperazine-1-carboxylic acid tert-butyl esterHCID 66823688—
Lösungsmittel1,2-DichloroethaneHCID 11—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTrifluoroacetic acidHCID 6422—
Produkt3-(3-Oxo-4-pyrimidin-2-yl-piperazin-1-yl)-azetidine-1-carboxylic acid tert-butyl esterHCID 6683624910,5%

Reaktionsschritte

A solution of intermediate 3b (120 mg, 0.43 mmol) in TFA (0.75 mL) and CH2Cl2 (3 mL) was stirred at room temperature for 1.5 h. The solution was concentrated. The resulting residue was stirred with N-Boc-azetidin-3-one 1a (81 mg, 0.47 mmol) and Na(OAc)3BH (100, 0.47 mmol) in 1,2-dichloroethane (4 mL) and HOAc (0.2 mL) at room temperature overnight. The reaction was quenched with aq. NaHCO3. The resulting mixture was extracted with CH2Cl2. The organic solution was dried over Na2SO4 and concentrated. Purification by column chromatography (silica gel, 3% MeOH/CH2Cl2) gave intermediate 3c as light yellow solid (15 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08637498B2
Quelldatensatzuspto-grants-2014_01
ORD IDord-e2272eb4ff46483387dd6f0643ba0185
Quellennotizuspto-grants-2014_01