Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
2-Cyanoethyl tetraisopropylphosphorodiamidite → Deoxyguanosine
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 2-Cyanoethyl tetraisopropylphosphorodiamidite | HCID 128153 | — |
| 반응물 | Acetonitrile methylene chloride | HCID 21877088 | — |
| 반응물 | 5'-O-p-Nitrobenzoyl-2-N-t-Butylphenoxyacetyldeoxyguanosine | HCID 137182965 | — |
| 반응물 | HCID 178458033 | HCID 178458033 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | Deoxyguanosine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06187914B1 |
| 출처 데이터셋 | uspto-grants-2001_02 |
| ORD ID | ord-c540f90c253c486fbbbc4a3f8e2d1e0b |
| 출처 메모 | uspto-grants-2001_02 |