Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | 1-Hexene | HCID 11597 | — |
| Reactant | HCID 86592813 | HCID 86592813 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 69538213 | HCID 69538213 | — |
Reaction Steps
The reaction was performed with 2-iodo-8-ethylaminoadenosine (8, 740 mg, 1.70 mmol) and (E)-1-borocatechol)-1-hexene (5.09 mmol). The mixture was purfied by column chromatography (10–20% MeOH in CH2Cl2).Yield 23 mg (0.06 mmol, 5%), mp 128–130÷C; Rƒ 0.61 (20% MeOH in CH2Cl2); 1H NMR (MeOD-d4) δ 6.92–6.82 (m, 1H, ═CHCH2), 6.29 (d, 1H, J=14.04 Hz, ═CH), 6.02 (d, 1H, J =7.64 Hz<H-1′), 4.80–4.76 (m, 1H, H-2′), 4.29–4.27 (m, 1H, H-3′), 4.13–4.11 (m, 1H, H4′), 3.81 (q, 2H, J=10.89 Hz, H-5′), 3.42 (q, 2H, J=6.02 Hz, NHCH2), 2.24 (q, 2H, J=6.00 Hz, ═CHCH2), 1.53–1.33 (m, 4H, CH2CH2), 1.28 (t, 3H, J=7.72 Hz, NHCH2CH3), 0.94 (t, 3H, J=7.11 Hz, CH3); MS m/z 393 (M+H)+; HPLC, System A: 20–100% CH3CN in H2O in 35 min., retention time=7.42 min.; System B: 30–100% CH3OH in H2O in 40 min., retention time=20.16 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07112574B2 |
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| Source dataset | uspto-grants-2006_09 |
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| ORD ID | ord-62e11299d8bd4d5799f5d441b26a603e |
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| Source note | uspto-grants-2006_09 |
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