HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Amino-4,6-dichloropyrimidine → tert-Butyl 4-(5-amino-6-chloropyrimidin-4-yl)piperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Amino-4,6-dichloropyrimidine | HCID 79434 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | tert-Butyl 4-(5-amino-6-chloropyrimidin-4-yl)piperazine-1-carboxylate | HCID 71748362 | 99.3% |
Reaction Steps
To a solution of 4,6-dichloro-5-aminopyrimidine (1 g, 6.1 mmol) in TEA (2 mL) and toluene (10 mL) was added 1-Boc-piperazine (2.3 g, 12.3 mmol). The mixture was refluxed for 12 hours. The solvent was removed and the residue was subject to chromatography on silica gel to afford the product 4-(5-amino-6-chloropyrimidin-4-yl)-piperazin-1-carboxylic acid tert-butyl ester (1.9 g, 99%). 1H NMR (CDCl3, 400 Hz) δ 8.16 (s, 1H), 3.87 (s, 2H), 3.56 (m, 4H), 3.29 (m, 4H), 1.49 (s, 9H). MS (ESI+) [M+H]+ 314.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08680114B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-85cf74fa945940f08f2d39f2f9d0f5ae |
| Source note | uspto-grants-2014_03 |