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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 895100생성일: 2026년 10월 26일

Triethylamine → (2R,3R,4R,5R)-4-acetyloxy-5-(acetyloxymethyl)-2-[2-iodo-6-(methoxyamino)purin-9-yl]oxolan-3-yl acetate

https://huagongshe.com/reaction/895100

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Acetic acid (2R,3R,4R,5R)-3,4-diacetoxy-5-(6-chloro-2-iodo-purin-9-YL)-tetrahydro-furan-2-ylmethyl esterHCID 482588—
반응물O-Methylhydroxylamine hydrochlorideHCID 521874—
용매TetrahydrofuranHCID 8028—
생성물(2R,3R,4R,5R)-4-acetyloxy-5-(acetyloxymethyl)-2-[2-iodo-6-(methoxyamino)purin-9-yl]oxolan-3-yl acetateHCID 16115476—

반응 단계

(2R,3R,4R,5R)-4-acetyloxy-5-(acetyloxymethyl)-2-(6-chloro-2-iodopurin-9-yl)oxolan-3-yl acetate (3.71 mmol) in dry tetrahydrofuran (60ml) was mixed with O-methyl hydroxylamine hydrochloride (37.1 mmol) and triethylamine (6.2 mL). The mixture was stirred at room temperature for 96 hours under an atmosphere of nitrogen. The solvent was removed in vacuo and the residue chromatographed on a flash silica gel column eluting with CHCl3—CH3OH (99:1), to give (2R,3R,4R,5R)-4-acetyloxy-5-(acetyloxymethyl)-2-[2-iodo-6-(methoxyamino)purin-9-yl]oxolan-3-yl acetate, a compound of formula (4), which was crystallized from a mixture of chloroform/hexanes (1:1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06914053B2
출처 데이터셋uspto-grants-2005_07
ORD IDord-d76a1ab68d464322a4e5d1900c8389ca
출처 메모uspto-grants-2005_07