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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1943418생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1943418

반응식

참여 물질

역할이름HCID투입량
반응물4-Amino-6-chloropyrimidineHCID 238012—
반응물Sodium benzyloxideHCID 23676753—
생성물6-(Benzyloxy)pyrimidin-4-amineHCID 30933827%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08389527B2
출처 데이터셋uspto-grants-2013_03
ORD IDord-d7104f18a0364c30a7071d4f90bfc1f0
출처 메모uspto-grants-2013_03