참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Diisopropylethylamine | HCID 81531 | — |
| 반응물 | Retinol | HCID 445354 | — |
| 반응물 | Sodium Bicarbonate | HCID 516892 | — |
| 반응물 | Phosphoramidite | HCID 10080320 | — |
| 반응물 | 2-Cyanoethyl-n,n-diisopropylchlorophosphoramidate | HCID 15927910 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 용매 | Triethylamine | HCID 8471 | — |
| 생성물 | Retinol phosphoramidite | HCID 131722191 | — |
반응 단계
All-trans-retinol (1 g) was vacuum dried and dissolved in anhydrous CH2Cl2 (10 ml) in an argon atmosphere. Diisopropylethylamine (2.65 ml, 21.5 mmol) was syringed in and the reaction mixture was cooled in an ice-bath. 2-cyanoethyl-N,N-diisopropylchlorophosphoramidate (2.5 g, 2.45 ml, 10.5 mmol) was slowly added by syringe under argon atmosphere. The reaction mixture was stirred for 30 min. at which time TLC (CH2Cl2:CH3OH:Et3N, 90:10:0.1) indicated complete conversion of the alcohol to its phosphoramidite. The reaction mixture was added to 100 ml of saturated NaHCO3 followed by washing the reaction flask with (2×25 ml) CH2Cl2. The CH2Cl2 layer was separated and washed with 100 ml of saturated NaCl solution and dried over anhydrous MgSO4 and evaporated into a yellow foam. The amidite was used directly in the DNA synthesizer without further purification since decomposition of this amidite was noted upon silica column purification.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07122649B2 |
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| 출처 데이터셋 | uspto-grants-2006_10 |
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| ORD ID | ord-f9d8db6e4ab94da683052f52397a2358 |
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| 출처 메모 | uspto-grants-2006_10 |
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