HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 20377607, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Diisopropyl Ether | HCID 7914 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 135737545 | HCID 135737545 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 20377607 | HCID 20377607 | — |
Reaction Steps
To a suspension of 0.4 g of 7-chloro-4,5-dihydro-5-phenyltetrazolo[1,5-a]quinazoline in 20 ml of dimethylformamide was added 0.07 g of 50% sodium hydride. After the mixture was stirred at room temperature for 1 hour, 0.4 g of methyl iodide was added thereto. The resulting mixture was stirred at room temperature for 2 hours and then poured into ice-water. The mixture was stirred with a small quantity of isopropyl ether, and the resulting precipitate was collected by filtration, washed successively with water and isopropyl ether, and dried to give 0.26 g of 7-chloro-4,5-dihydro-4-methyl-5-phenyltetrazolo[1,5-a]quinazoline as pale yellow crystals. Recrystallization from ethanol gave colorless scales, m.p. 282°-283° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04183932 |
| Source dataset | uspto-grants-1980_01 |
| ORD ID | ord-5d36718361e84b058d9969988ed0755a |
| Source note | uspto-grants-1980_01 |