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HRID 1943418作成日:2026年10月26日

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

https://huagongshe.com/reaction/1943418

反応式

関与物質

役割名称HCID仕込み量
反応物4-Amino-6-chloropyrimidineHCID 238012—
反応物Sodium benzyloxideHCID 23676753—
生成物6-(Benzyloxy)pyrimidin-4-amineHCID 30933827%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08389527B2
出典データセットuspto-grants-2013_03
ORD IDord-d7104f18a0364c30a7071d4f90bfc1f0
出典メモuspto-grants-2013_03