참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 1-Iodooctadecane | HCID 12402 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 2-Aminoadenosine | HCID 72200 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 2,6-Diamino-9-(2-O-octadecyl-beta-D-ribofuranosyl)purine | HCID 11731187 | 11.4% |
반응 단계
2,6-Diamino-9-(β-D-ribofuranosyl)purine (50 g, 180 mmol) and sodium hydride (7 g) in DMF (1 l) were heated to boiling for 2 hr. Iodooctadecane (100 g) was added at 150° C. and the reaction mixture allowed to cool to RT. The reaction mixture was stirred for 11 days at RT. The solvent was evaporated and the residue purified by silica gel chromatography. The product was eluted with 5% MeOH/CH2Cl2. The product containing fraction were evaporated to yield the product (11 g). 1H NMR (DMSO-d6) δ 0.84 (t, 3, CH2); 1.22 [m, 32, O--CH2 --CH2 --(CH2)16 --]; 1.86 (m, 2, O--CH2CH2 --); 3.25 (m, 2, O--CH2 --); 3.93 (d, 1, 4'H), 4.25 (m, 1, 3'H); 4.38 (t, 1, 2'H); 5.08 (d, 1, 3'-OH); 5.48 (t, 1, 5'-OH); 5.75 (s, 2, 6-NH2); 5.84 (d, 1, 1'-H); 6.8 (s, 2, 2-NH2); and 7.95 (s, 1, 8-H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US06133438 |
|---|
| 출처 데이터셋 | uspto-grants-2000_10 |
|---|
| ORD ID | ord-0bc1e61b368343588b8e2f9ae006fec7 |
|---|
| 출처 메모 | uspto-grants-2000_10 |
|---|