HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → Methyl 2-(3-chlorobenzyl)-4-oxo-3,4-dihydroquinazoline-7-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | m-Chlorophenylacetonitrile | HCID 73722 | — |
| Reactant | Dimethyl aminoterephthalate | HCID 79336 | — |
| Reactant | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| Product | Methyl 2-(3-chlorobenzyl)-4-oxo-3,4-dihydroquinazoline-7-carboxylate | HCID 136330125 | 67.9% |
Reaction Steps
A mixture of 628 mg of dimethyl aminoterephthalate, 546 mg of 3-chlorophenylacetonitrile and 15 mL of 4N hydrogen chloride dioxane solution was stirred at room temperature for 7 hours. Further continuing the stirring at 30° C. for 63 hours and at 70° C. for 25 hours, ice was added to the reaction mixture, followed by addition of 7 mL of 25% aqueous ammonia. Whereupon precipitated crystals were recovered by filtration, and washed with water, ether and chloroform by the order stated. Subjecting the crystals to through-flow drying under heating, 670 mg of the title compound was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08101624B2 |
| Source dataset | uspto-grants-2012_01 |
| ORD ID | ord-d0a4eba0fc884d528c766ca2cd67e528 |
| Source note | uspto-grants-2012_01 |