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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 271260생성일: 2026년 10월 26일

2-Cyclohexylethanol → 9-(2-Cyclohexylethyl)-6-(2-furyl)-9H-purine-2-amine

https://huagongshe.com/reaction/271260

반응식

참여 물질

역할이름HCID투입량
반응물2-CyclohexylethanolHCID 20508—
반응물Di-tert-butyl azodicarboxylateHCID 97268—
반응물6-(furan-2-yl)-9H-purin-2-amineHCID 178508247—
용매DimethylformamideHCID 6228—
용매TetrahydrofuranHCID 8028—
생성물9-(2-Cyclohexylethyl)-6-(2-furyl)-9H-purine-2-amineHCID 5983509858.9%

반응 단계

A solution of 6-(2-furyl)-1H-purine-2-amine (25 mg, 0.12 mmol) in anhydrous DMF (0.5 mL) and anhydrous THF (2 mL) was treated with triphenylphosphine polystyrene (65 mg, 0.25 mmol) and 2-cyclohexylethanol (35 mg, 0.25 mmol), shaken at room temperature for 10 min, treated with di-tert-butyl azodicarboxylate (0.058 g, 0.25 mmol), shaken at room temperature for 16 h, filtered and concentrated in vacuo. The resulting oil was dissolved in CH2Cl2 (2 mL) and TFA (1 mL), shaken for 2 h and concentrated in vacuo. The resulting oil was dissolved in CH2Cl2 (3 mL), shaken with 1-M aq HCl (1 mL) for 15 min and the organic phase concentrated in vacuo and purified by chromatography (SiO2; EtOAc) to give the title compound (22 mg, 57%) as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07452894B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-d26ba319f471470d8cfa8588437719c1
출처 메모uspto-grants-2008_11