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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1030775생성일: 2026년 10월 26일

Acetonitrile → 5'-O-acetyl-2',3'-dideoxyadenosine

https://huagongshe.com/reaction/1030775

반응식

참여 물질

역할이름HCID투입량
반응물AcetonitrileHCID 6342—
반응물1,1'-Diheptyl-4,4'-bipyridinium dibromideHCID 80262—
반응물9-(2,5-di-O-acetyl-3-bromo-3-deoxy-beta-D-xylofuranosyl)adenineHCID 10982560—
반응물HCID 178418361HCID 178418361—
촉매HCID 178418390HCID 178418390—
용매TriethylamineHCID 8471—
생성물((2S,5R)-5-(6-Amino-9H-purin-9-yl)-2,5-dihydrofuran-2-yl)methyl acetateHCID 11022122—
생성물5'-O-acetyl-2',3'-dideoxyadenosineHCID 1498946711%
생성물2',5'-di-O-acetyl-3'-deoxyadenosineHCID 149894683%

반응 단계

To 120 ml of acetonitrile were added 1.50 g (3.62 mmols) of 9-(2,5-di-O-acetyl-3-bromo-3-deoxy-β-D-xylofuranosyl) adenine, 946 mg (1.84 mmol) of N,N'-diheptyl-4,4'-bipyridinium dibromide, 1.13 g of 10% palladium-carbon (water content, 50%) and 2.5 ml of triethylamine. The mixture was stirred for 2 hours at room temperature in a hydrogen atmosphere. The analysis by HPLC reveals that the raw material disappeared and 5'-O-acetyl-2',3'-didehydro-2',3'-dideoxyadenosine (85), 5'-O-acetyl-2',3'-dideoxyadenosine (11%) and 2',5'-di-O-acetyl-3'-deoxyadenosine (3%) were formed.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05106962
출처 데이터셋uspto-grants-1992_04
ORD IDord-ae99ac58e91b4559a1428c60995f923b
출처 메모uspto-grants-1992_04