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2-Cyanoethyl tetraisopropylphosphorodiamidite → Deoxyadenosine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | 2-Cyanoethyl tetraisopropylphosphorodiamidite | HCID 128153 | — |
| 反応物 | 5'-o-p-Nitrobenzoyl-6-n-phenoxyacetyldeoxyadenosine | HCID 15382694 | — |
| 反応物 | Acetonitrile methylene chloride | HCID 21877088 | — |
| 反応物 | HCID 178458033 | HCID 178458033 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | Deoxyadenosine | HCID 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
| 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-6625e8aedc394629bd66356b7ecbe40a |
| 出典メモ | uspto-grants-2001_02 |