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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 232365생성일: 2026년 10월 25일

Carbon tetrabromide → 5'-Azido-2',5'-dideoxy-5-(2-chloroethyl)uridine

https://huagongshe.com/reaction/232365

반응식

참여 물질

역할이름HCID투입량
반응물Carbon tetrabromideHCID 11205—
반응물TriphenylphosphineHCID 11776—
반응물Lithium azideHCID 88163—
반응물5-(2-Chloroethyl)-2'-deoxyuridineHCID 514814—
용매MethanolHCID 887—
용매DimethylformamideHCID 6228—
생성물5'-Azido-2',5'-dideoxy-5-(2-chloroethyl)uridineHCID 5400230731.6%

반응 단계

1.4 g of 5-(2-chloroethyl)-2'-deoxyuridine and 1.3 g of triphenylphosphine were dissolved in 20 ml of dimethylformamide and stirred while 1.2 g of lithium azide were added to give a solution within 5 minutes at room temperature. 1.7 g of carbon tetrabromide were added portionwise during 5 minutes to give a hazy orange colored solution which was stirred at room temperature for 17 hours. 5 ml of methanol were added to give a clear solution. After 0.5 hour, the solvents were removed by evaporation under an oil pump vacuum to give a gum which was partitioned between 30 ml of ethyl acetate and 20 ml of water. The white solid which formed was removed by filtration to give 0.64 g of crude product of melting point 179°-182° C. (decomposition). This crude product was stirred with methanol and then removed by filtration to give 0.48 g of pure 5'-azido-2',5'-dideoxy-5-(2-chloroethyl)-uridine of melting point 197°-199° C. (decomposition).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04851519
출처 데이터셋uspto-grants-1989_07
ORD IDord-104589e5e70540d595c331276c191bfc
출처 메모uspto-grants-1989_07