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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 635504생성일: 2026년 10월 25일

2-Cyanoethyl tetraisopropylphosphorodiamidite → Deoxyguanosine

https://huagongshe.com/reaction/635504

반응식

참여 물질

역할이름HCID투입량
반응물2-Cyanoethyl tetraisopropylphosphorodiamiditeHCID 128153—
반응물Acetonitrile methylene chlorideHCID 21877088—
반응물5'-O-p-Nitrobenzoyl-2-N-t-ButylphenoxyacetyldeoxyguanosineHCID 137182965—
반응물HCID 178458033HCID 178458033—
용매DichloromethaneHCID 6344—
생성물DeoxyguanosineHCID 135398592—

반응 단계

5′-O-p-nitrobenzoyl-2-N-t-butylphenoxyacetyldeoxyguanosine (1 eq) is dried in a dichloromethane/acetonitrile mixture and reacted with 1.2 eq of bisdiisopropylaminocyanoethoxyphosphine and 0.5 eq of diisopropylammoniumtetrazolide in anhydrous dichloromethane. After reacting for 2 hours, the reaction mixture is diluted and washed successively with 0.5 M sodium bicarbonate and saturated sodium chloride. The organic phase is evaporated to dryness. After redissolution in chloroform and precipitation in hexane, the product is dried under vacuum and stored under argon. This amidite is soluble in acetonitrile, a solvent in which oligonucleotide syntheses are conventionally carried out.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06187914B1
출처 데이터셋uspto-grants-2001_02
ORD IDord-c540f90c253c486fbbbc4a3f8e2d1e0b
출처 메모uspto-grants-2001_02