HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dioxane → 2-(4-Cyclohexylthiocarbamoyl-piperazin-1-yl)-4-amino-6,7-dimethoxyquinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Cyclopentyl isothiocyanate | HCID 141792 | — |
| Reactant | 2-(1-Piperazinyl)-4-amino-6,7-dimethoxyquinazoline | HCID 616267 | — |
| Product | 2-(4-Cyclohexylthiocarbamoyl-piperazin-1-yl)-4-amino-6,7-dimethoxyquinazoline | HCID 13714098 | — |
Reaction Steps
To a solution prepared by dissolving 868 mg. (3 mmole) of 2-piperazine-4-amino-6,7-dimethoxyquinazoline in 30 ml of dioxane, there was added dropwise 424 mg. (13 mmole) of cyclopentyl isothiocyanate at room temperature. The mixture was stirred overnight at room temperature. After evaporation of the solvent from the reaction mixture, the residue was chromatographed on silica gel, and eluted with 2% ethanol-chloroform to obtain 1.26 g. of the desired product. The product was dissolved in 10 ml of iso-propanol and 2 ml of 2N hydrochloric acid was added to the resultant solution to form a hydrochloride, which was in turn isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04607034 |
| Source dataset | uspto-grants-1986_08 |
| ORD ID | ord-f06bd359ea864ba6a5b36344d25835d1 |
| Source note | uspto-grants-1986_08 |