HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Butanol → 2-Chloro-N-(4-methoxybenzyl)-9H-purin-6-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Butanol | HCID 263 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2,6-Dichloropurine | HCID 5324412 | — |
| Reactant | Benzyl(methoxy)amine | HCID 11815413 | — |
| Product | 2-Chloro-N-(4-methoxybenzyl)-9H-purin-6-amine | HCID 16422056 | — |
Reaction Conditions
| Temperature | 120 °C |
|---|
Reaction Steps
The 2,6-dichloropurine (4.06 g, 21.5 mmol) was suspended in n-butanol (150 ml) and the 4 methoxybenzylamine was added (3.4 ml, 26 mmol). The solution turned clear and then cloudy a few minutes later. The solution was heated at 120° C. for 2 hr and then cooled. The n-butanol was evaporated followed by suspension of the residue in water and diethyl ether mixture. A solution of 2N NaOH (1.3 ml, 26 mmol) was added and the solution stirred for 10 min before filtration. The filtered precipitate was washed with water and a small portion of ether and then dried under vacuum. The residual liquor was left overnight and more crystals were collected the next day and washed with diethyl ether.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06790958B2 |
| Source dataset | uspto-grants-2004_09 |
| ORD ID | ord-ac1b782227a94241b45ebbae43423cff |
| Source note | uspto-grants-2004_09 |