HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloro-6,7-dimethoxy-4-quinazolinamine → HCID 131712025, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloro-6,7-dimethoxy-4-quinazolinamine | HCID 90235 | — |
| Reactant | 3-(Piperidin-4-yl)propanoic acid--hydrogen chloride (1/1) | HCID 21198547 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 131712025 | HCID 131712025 | 114.7% |
Reaction Steps
4-Amino-2-chloro-6,7-dimethoxyquinazoline (24.9 g) and 3-(4-piperidinyl)propionic acid, hydrochloride (20 g) in n-butanol (1000 ml) were stirred under reflux for 20 hours. The hot suspension was filtered and the insoluble material discarded. The filtrate was cooled in ice/water, the precipitated solid collected and the filtrate evaporated in vacuo. The resulting solid and the precipitated solid were combined and crystallised from isopropanol to give 4-amino-2-[4-(2-{n-butoxycarbonyl}ethyl)piperidino]-6,7-dimethoxyquinazoline, hydrochloride (27.0 g) with m.p. 250°-252°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04243666 |
| Source dataset | uspto-grants-1981_01 |
| ORD ID | ord-741510022d514c349793c795e552878b |
| Source note | uspto-grants-1981_01 |