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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 368715생성일: 2026년 10월 26일

1-Iodooctadecane → 2,6-Diamino-9-(2-O-octadecyl-beta-D-ribofuranosyl)purine

https://huagongshe.com/reaction/368715

반응식

참여 물질

역할이름HCID투입량
반응물1-IodooctadecaneHCID 12402—
반응물Sodium hydrideHCID 24758—
반응물2-AminoadenosineHCID 72200—
용매DimethylformamideHCID 6228—
생성물2,6-Diamino-9-(2-O-octadecyl-beta-D-ribofuranosyl)purineHCID 1173118711.4%

반응 단계

2,6-Diamino-9-(β-D-ribofuranosyl)purine (50 g, 180 mmol) and sodium hydride (7 g) in DMF (1 l) were heated to boiling for 2 hr. Iodooctadecane (100 g) was added at 150° C. and the reaction mixture allowed to cool to RT. The reaction mixture was stirred for 11 days at RT. The solvent was evaporated and the residue purified by silica gel chromatography. The product was eluted with 5% MeOH/CH2Cl2. The product containing fraction were evaporated to yield the product (11 g). 1H NMR (DMSO-d6) δ 0.84 (t, 3, CH2); 1.22 [m, 32, O--CH2 --CH2 --(CH2)16 --]; 1.86 (m, 2, O--CH2CH2 --); 3.25 (m, 2, O--CH2 --); 3.93 (d, 1, 4'H), 4.25 (m, 1, 3'H); 4.38 (t, 1, 2'H); 5.08 (d, 1, 3'-OH); 5.48 (t, 1, 5'-OH); 5.75 (s, 2, 6-NH2); 5.84 (d, 1, 1'-H); 6.8 (s, 2, 2-NH2); and 7.95 (s, 1, 8-H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06133438
출처 데이터셋uspto-grants-2000_10
ORD IDord-0bc1e61b368343588b8e2f9ae006fec7
출처 메모uspto-grants-2000_10