HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodine → 2-(4-Chlorophenyl)-5-iodopyrazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodine | HCID 807 | — |
| Reactant | Tert-Butyl nitrite | HCID 10906 | — |
| Reactant | Sodium Thiosulfate | HCID 24477 | — |
| Reactant | 5-(4-Chlorophenyl)pyrazin-2-amine | HCID 20567029 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Carbon Tetrachloride | HCID 5943 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(4-Chlorophenyl)-5-iodopyrazine | HCID 85969636 | — |
Reaction Steps
With the exclusion of light, 4.9 mL (40.0 mmol) tert-butylnitrite and 7.6 g (30 mmol) iodine are added to a solution of 4.8 g (23.3 mmol) 5-(4-chloro-phenyl)-pyrazin-2-ylamine in 100 mL CCl4 and 50 mL DCM and the reaction mixture is stirred overnight at RT. It is combined with 100 mL water and 50 mL 10% Na2S2O3 solution, the organic phase is separated off, washed again with 50 mL 10% Na2S2O3 solution and twice with 50 mL water and dried over MgSO4. It is filtered through activated charcoal, evaporated down i.vac. and the residue is purified by chromatography (silica gel, gradient: PE to PE/EtOAc 8:2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08618132B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-b737f8bc55244498810f760a7d37b76a |
| Source note | uspto-grants-2013_12 |