HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloroisatoic anhydride → 7-Chloro-3-[4-(1H-imidazol-1-yl)butyl]-4(3H)-quinazolinone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloroisatoic anhydride | HCID 329105 | — |
| Reactant | HCID 178510959 | HCID 178510959 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7-Chloro-3-[4-(1H-imidazol-1-yl)butyl]-4(3H)-quinazolinone | HCID 13952825 | — |
Reaction Steps
A mixture of 1.39 g of imidazole-4-butanamine, 1.98 g of 4-chloroisatoic anhydride and 25 ml of ethanol was left at room temperature for 20 hours and concentrated. The residue and 5 ml of triethyl orthoformate were heated in an oil bath at 100°-125° C. for 3 hours and concentrated. The mixture was treated with ether to obtain the desired product, mp 123°-125° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04753944 |
| Source dataset | uspto-grants-1988_06 |
| ORD ID | ord-00a6a36566784e918a75db289e5621d2 |
| Source note | uspto-grants-1988_06 |