HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosphorus pentachloride → 4-Chloro-2-(1-methyl-5-nitro-1H-imidazol-2-yl)quinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosphorus pentachloride | HCID 24819 | — |
| Reactant | 2-(1-Methyl-5-nitro-1H-imidazol-2-yl)quinazolin-4(1H)-one | HCID 135727391 | — |
| Solvent | Phosphorus oxychloride | HCID 24813 | — |
| Product | 4-Chloro-2-(1-methyl-5-nitro-1H-imidazol-2-yl)quinazoline | HCID 21402096 | — |
Reaction Steps
A suspension of 25 g of 2-(1-methyl-5-nitro-2-imidazolyl)-4-quinazolinone and 26.2 g of phosphorus pentachloride in 150 ml of phosphorus oxychloride is boiled for 3 hours and then evaporated in vacuo (12 Torr). The residue is taken up in methylene chloride and stirred with water for one hour at room temperature. The mixture is made alkaline with sodium bicarbonate and extracted by dropwise addition of methylene chloride. The mixture is dried with magnesium sulphate and treated with animal charcoal, filtered and evaporated in vacuo (12 Torr) at 30° C. The residue is mixed with ether, filtered and washed pure with ether to obtain the heading compound, m.p. 178°-181° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04055642 |
| Source dataset | uspto-grants-1977_10 |
| ORD ID | ord-62279d4f02cf488fb8b4a6ae26723e95 |
| Source note | uspto-grants-1977_10 |