HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 8-(4-Bromobenzylamino)adenosine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 8-Bromoadenosine | HCID 96544 | — |
| Reactant | 4-Bromobenzylamine hydrochloride | HCID 2724096 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 8-(4-Bromobenzylamino)adenosine | HCID 67455531 | 90.5% |
Reaction Steps
A mixture of 8-bromoadenosine (0.100 g), 4-bromobenzylamine hydrochloride (0.193 g) and triethylamine (0.201 mL) in ethanol (2.9 mL) was stirred under reflux for 96 hours. The reaction mixture was cooled to room temperature and concentrated under reduced pressure. The residue was purified by column chromatography on aminopropylated silica gel (eluent: dichloromethane/methanol=10/1) to give the title compound (0.118 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07795236B2 |
| Source dataset | uspto-grants-2010_09 |
| ORD ID | ord-639b01dafef94996920f61aa46db08fb |
| Source note | uspto-grants-2010_09 |