HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-(1-Azidoethyl)-5-fluoropyrimidine → 1-(5-Fluoropyrimidin-2-yl)ethan-1-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-(1-Azidoethyl)-5-fluoropyrimidine | HCID 50993723 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Product | 1-(5-Fluoropyrimidin-2-yl)ethan-1-amine | HCID 50994814 | 99% |
Reaction Steps
A round-bottom flask containing 2-(1-azidoethyl)-5-fluoropyrimidine (Method 3, 0.60 g, 3.59 mmol) was charged with 10% Pd/C (0.191 g) and was evacuated and backfilled with H2 via a filled balloon. MeOH (10 ml) was added, and the mixture was allowed to stir at room temperature for 3 hours. The mixture was filtered through a plug of diatomaceous earth, which was subsequently washed well with MeOH. The filtrates were concentrated to give the title compound as a pale yellow oil (0.50 g, 99%). 1H NMR (CDCl3) δ 8.60 (s, 2H), 4.65 (br s 2H), 4.10 (m, 1H), 1.20 (d, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08088784B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-0f9993312b8f447b9a64c7f2ca1fdee8 |
| Source note | uspto-grants-2012_01 |