Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Hexyne | HCID 12732 | — |
| Reactant | 7-DEAZA-7-IODO-2'-DEOXYGUANOSINE | HCID 135405252 | — |
| Catalyst | Copper iodide | HCID 83717 | — |
| Product | HCID 135678277 | HCID 135678277 | — |
Reaction Steps
Copper iodide (38.1 mg, 0.2 mmol), triethylamine (2.8 ml, 2 mmol), tetrakis(triphenylphsophine)palladium(0) (40.5 mg, 0.1 mmol) and 1-hexyne (492 mg, 6 mmol) are added to an argon-flushed solution of compound (58) (390 mg, 1 mmol in 5 ml of dried DMF), and the solution is stirred at room temperature for 24 h. It is then evaporated and the residue is loaded onto a silica gel column (5×25 cm). Title compound (65) is obtained following stepwise elution with 5%, 10% and 20% MeOH in CH2Cl2. Recrystallization from MeCN affords a colorless solid (120 mg, 35%). 1H-NMR ([(D6] DMSO): δ=0.94 (m, CH3), 1.49, 2.38 (m, CH2), 2.0 (M, Hα—C(2′)), 2.35 (m, Hβ—C(2′)), 3.50 (m, H2—C(5′)), 3.76 (m, H—C(4′)), 4. (m, H—C(3′)), 4.88 (t, 5′-OH), 5.18 (d, J=3.5, 3′-OH), 6.27 (m, H—C(1′) +NH2), 7.13 (s, H—C(6)), 10.34 (br., NH). MS: m/e 346 (M+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06479651B1 |
|---|
| Source dataset | uspto-grants-2002_11 |
|---|
| ORD ID | ord-d223583dae1645c8a08ff5e4c0995c23 |
|---|
| Source note | uspto-grants-2002_11 |
|---|