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2-Cyanoethyl tetraisopropylphosphorodiamidite → Deoxyguanosine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Cyanoethyl tetraisopropylphosphorodiamidite | HCID 128153 | — |
| 反応物 | Acetonitrile methylene chloride | HCID 21877088 | — |
| 反応物 | 5'-O-p-Nitrobenzoyl-2-N-t-Butylphenoxyacetyldeoxyguanosine | HCID 137182965 | — |
| 反応物 | HCID 178458033 | HCID 178458033 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | Deoxyguanosine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US06187914B1 |
| 出典データセット | uspto-grants-2001_02 |
| ORD ID | ord-c540f90c253c486fbbbc4a3f8e2d1e0b |
| 出典メモ | uspto-grants-2001_02 |