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HRID 635499作成日:2026年10月26日

2-Cyanoethyl tetraisopropylphosphorodiamidite → Deoxyadenosine

https://huagongshe.com/reaction/635499

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5'-o-p-Nitrobenzoyl-6-n-phenoxyacetyldeoxyadenosineHCID 15382694—
反応物Acetonitrile methylene chlorideHCID 21877088—
反応物HCID 178458033HCID 178458033—
溶媒DichloromethaneHCID 6344—
生成物DeoxyadenosineHCID 13730—

反応手順

5′-O-p-Nitrobenzoyl-6-N-phenoxyacetyldeoxyadenosine (1 eq) is dried in a dichloromethane/acetonitrile mixture and reacted with 1.2 eq of bisdiisopropylaminocyanoethoxyphosphine and 0.5 eq of diisopropylammonium tetrazolide 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 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-6625e8aedc394629bd66356b7ecbe40a
出典メモuspto-grants-2001_02