HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-([1,1′-Biphenyl]-4-ylmethyl)-2-chloro-9H-purin-6-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Phenylbenzylamine | HCID 344989 | — |
| Reactant | 2,6-Dichloropurine | HCID 5324412 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | N-([1,1′-Biphenyl]-4-ylmethyl)-2-chloro-9H-purin-6-amine | HCID 21951838 | 99% |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
The 2,6-dichloropurine (5.0 g, 26.45 mmol) was suspended in n-butanol (50 ml) and the 4-phenylbenzylamine (6.61 g, 29.1 mmol) and triethylamine (4.1 ml, 29.1 mmol) were added. The solution was heated at 120° C. overnight then cooled. Filtered off product using excess n-butanol and washed precipitate with 100 ml 1M HCl and 200 ml water. The solid was dried in vaccum over overnight at 70° C. to give the desired product as a pale yellow solid. Yield=99%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06794390B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-affb7cac8a014839a912d297c39378f3 |
| Source note | uspto-grants-2004_09 |