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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1943418Erstellt: 25. Oktober 2026

4-Amino-6-chloropyrimidine → 6-(Benzyloxy)pyrimidin-4-amine

https://huagongshe.com/reaction/1943418

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Amino-6-chloropyrimidineHCID 238012—
EduktSodium benzyloxideHCID 23676753—
Produkt6-(Benzyloxy)pyrimidin-4-amineHCID 30933827%

Reaktionsschritte

6-Chloropyrimidin-4-amine (500 mg, 3.86 mmol) and sodium phenylmethanolate (1 M solution in benzyl alcohol, 4.67 mL, 4.67 mmol) were heated at 120° C. for 16 hrs. 6-(Benzyloxy)pyrimidin-4-amine (210 mg, 27% yield) was isolated as clear oil following HPLC purification (Phenomenex Axia Luna 5 micron 30×100 mm) 30% B (Solvent B=90% MeOH-10% H2O-0.1% TFA) to 100% B in A (Solvent A=10% MeOH-90% H2O-0.1% TFA). The purified material (a TFA salt) was converted to its free base by dissolving in ethyl acetate (20 mL) and washing with saturated NaHCO3 (20 mL) for use in the next step. LC/MS (Phenomenex Luna 5 micron C18 4.6×30 mm, 0 to 100 B in 2 min with 1 min hold time, Flow rate=5 mL/min, detection at 254 nm, Solvent A: 10% methanol/90% water/0.1% TFA; Solvent B: 10% water/90% methanol/0.1% TFA). Rt=0.96 (M+H=202.24).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08389527B2
Quelldatensatzuspto-grants-2013_03
ORD IDord-d7104f18a0364c30a7071d4f90bfc1f0
Quellennotizuspto-grants-2013_03