HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 5-Iodo-2-(piperazin-1-yl)pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 2-Chloro-5-iodopyrimidine | HCID 1714223 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Iodo-2-(piperazin-1-yl)pyrimidine | HCID 15729876 | — |
Reaction Steps
0.02 mol of 2-chloro-5-iodopyrimidine, 0.06 mol of piperazine and 100 ml of absolute dimethylformamide are heated to 100° for 45 minutes and then evaporated. The crystalline residue is shaken with potassium bicarbonate solution and methylene chloride. The substance contained in the methylene chloride phase is purified by column chromatography over silica gel 60. The amine obtained by elution with methylene chloride/methanol (7:3) is stirred with isopropyl ether and filtered off with suction.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04937343 |
| Source dataset | uspto-grants-1990_06 |
| ORD ID | ord-e687f32e07f74c639c66782c91aa894f |
| Source note | uspto-grants-1990_06 |