HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Benzylpiperazine → (4-Benzyl-piperazin-1-yl)-6-iodothieno[3,2-d]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Benzylpiperazine | HCID 75994 | — |
| Reactant | 4-Chloro-6-iodothieno(3,2-d)pyrimidine | HCID 46835550 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | (4-Benzyl-piperazin-1-yl)-6-iodothieno[3,2-d]pyrimidine | HCID 67540584 | 88.2% |
Reaction Steps
To a solution of 4-chloro-6-iodothieno[3,2-d]pyrimidine (0.5 g, 1.7 mmol) in DCE (5 mL)/TEA (1 mL) was added 1-Benzyl-piperazine (0.3 g, 1.69 mmol). The mixture was refluxed for 1 hour. The solvent was removed and the residue was subject to chromatography on silica gel to afford (4-Benzyl-piperazin-1-yl)-6-iodothieno[3,2-d]pyrimidine (0.65 g, 88%). 1H NMR (CDCl3, 400 Hz) δ 8.47 (s, 1H) 7.60 (s, 1H), 7.35-7.23 (m, 5H), 3.95-3.92 (m, 4H), 3.51 (s, 2H), 2.59-2.54 (m, 4H). MS (ESI+) [M+H]+ 437.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08680114B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-b30b93a2f35d408cb760ca402437edcc |
| Source note | uspto-grants-2014_03 |