HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → 8-hydroxymethyl-2-isopropoxy-11H-pyrido[2,1-b]quinazoline-11-one benzoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Triglyme | HCID 8189 | — |
| Reactant | 2-Amino-5-(propan-2-yloxy)benzoic acid | HCID 12719189 | — |
| Reactant | 6-Chloro-3-pyridinemethanol benzoate | HCID 13052311 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 8-hydroxymethyl-2-isopropoxy-11H-pyrido[2,1-b]quinazoline-11-one benzoate | HCID 20525675 | — |
Reaction Steps
A suspension of 1.0 g. of 5-isopropoxyanthranilic acid, 1.1 g. of 6-chloro-3-pyridinemethanol benzoate and 0.01 g. of potassium iodide in 10 ml. of triglyme was heated to 150° overnight under a stream of argon. On cooling, the reaction mixture was dissolved in hot methanol, filtered and evaporated to an orange oil. Chromatographic separation and recrystallization from hexane-dichloromethane yielded 8-hydroxymethyl-2-isopropoxy-11H-pyrido[2,1-b]quinazoline-11-one benzoate, mp 123°-126°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04348396 |
| Source dataset | uspto-grants-1982_09 |
| ORD ID | ord-a4bcd6a5ff19416282d1ea179452c622 |
| Source note | uspto-grants-1982_09 |