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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1882567생성일: 2026년 10월 25일

Diisopropylethylamine → N-((1S,2R,3S,4R)-4-{6-[2,2-Bis-(4-hydroxy-phenyl)-ethylamino]-2-chloro-purin-9-yl}-2,3-dihydroxy-cyclopentyl)-propionamide hydrochloride

https://huagongshe.com/reaction/1882567

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물4,4'-(2-Aminoethylidene)bisphenolHCID 21710280—
반응물[(1S,2R,3S,4R)-4-(2,6-dichloro-purin-9-yl)-2,3-dihydroxy-cyclopentyl]-propionyl-carbamic acid tert-butyl esterHCID 44140426—
용매TetrahydrofuranHCID 8028—
생성물N-((1S,2R,3S,4R)-4-{6-[2,2-Bis-(4-hydroxy-phenyl)-ethylamino]-2-chloro-purin-9-yl}-2,3-dihydroxy-cyclopentyl)-propionamide hydrochlorideHCID 86647554—

반응 단계

A reaction mixture comprising [(1S,2R,3S,4R)-4-(2,6-dichloro-purin-9-yl)-2,3-dihydroxy-cyclopentyl]-propionyl-carbamic acid tert-butyl ester (Intermediate G) (2.00 g, 4.35 mmol) and 4,4′-(2-aminoethylidene)bis-phenol (prepared by the procedure of R. M. Schelkun et al. Bioorg. Med. Chem. Lett. 9 (1999) 2447-2452.) (1.19 g, 5.20 mmol) in dry THF (40 ml) is treated with DIPEA (0.67 g, 5.20 mmol) and stirred at room temperature for 2 days. The solvent is removed in vacuo and the title compound is obtained after purification by reverse phase column chromatography (Isolute™ C18, 20-70% acetonitrile in water −0.1% HCl).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08318750B2
출처 데이터셋uspto-grants-2012_11
ORD IDord-6815395856ce45d1b40869e3937b17cf
출처 메모uspto-grants-2012_11