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HRID 635504作成日:2026年10月26日

2-Cyanoethyl tetraisopropylphosphorodiamidite → Deoxyguanosine

https://huagongshe.com/reaction/635504

反応式

関与物質

役割名称HCID仕込み量
反応物2-Cyanoethyl tetraisopropylphosphorodiamiditeHCID 128153—
反応物Acetonitrile methylene chlorideHCID 21877088—
反応物5'-O-p-Nitrobenzoyl-2-N-t-ButylphenoxyacetyldeoxyguanosineHCID 137182965—
反応物HCID 178458033HCID 178458033—
溶媒DichloromethaneHCID 6344—
生成物DeoxyguanosineHCID 135398592—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06187914B1
出典データセットuspto-grants-2001_02
ORD IDord-c540f90c253c486fbbbc4a3f8e2d1e0b
出典メモuspto-grants-2001_02