HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Iodoadenosine → 2-{3-[1-((4-Methyl)phenoxycarbanoyl)piperidin-4-yl]propyn-1-yl}adenosine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Iodoadenosine | HCID 169662 | — |
| Reactant | 4-Methylphenyl 4-(prop-2-ynyl)piperidine-1-carboxylate | HCID 57838914 | — |
| Product | 2-{3-[1-((4-Methyl)phenoxycarbanoyl)piperidin-4-yl]propyn-1-yl}adenosine | HCID 25094145 | — |
Reaction Steps
Batch: AB-10-019. 4-methylphenyl 4-(prop-2-ynyl)piperidine-1-carboxylate, batch JR28-105 (0.548 g, 2.130 mmol) was added to a solution of 2-iodoadenosine (0.629 g, 1.600 mmol) according to general procedure 2. Yield: 0.236 g, 28%. 1H NMR (CD3OD) δ 8.29 (s, 1H), 7.14-6.92 (2×m, 4H), 5.95 (d, 1H), 4.75 (m, 2H), 4.34-4.16 (2×m, 3H), 3.91-3.71 (2×d, 2H), 3.10-2.90 (2×bt, 4H), 2.28 (s, 3H), 2.43 (d, 5H), 1.92-1.41 (2×m, 5H). m/z MH+=523.16. HPLC rt=6.8 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07888329B2 |
| Source dataset | uspto-grants-2011_02 |
| ORD ID | ord-5a9bd11a8c9e4f7893004a6a32d053e0 |
| Source note | uspto-grants-2011_02 |