HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 86692087, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Quinazoline | HCID 9210 | — |
| Reactant | 4-Chloro-6-iodoquinazoline | HCID 11173809 | — |
| Reactant | HCID 57088589 | HCID 57088589 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 86692087 | HCID 86692087 | 40% |
Reaction Steps
0.75 g of 4-chloro-6-iodoquinazoline, 0.51 g of 2,3,4a,8a-tetrahydro-1H-quinolin-4-one and 0.96 ml of triethylamine in 5 ml of dioxane are heated at 80° C. in a flask until the quinazoline has reacted completely (HPLC check, about 24 hours). The cooled reaction solution is diluted with EA and washed 3 times with water. The organic phase is dried over sodium sulfate and purified by means of column chromatography (gradient heptane: EA 5-100% in 16 min.), giving 0.40 g of 1-(6-iodoquinazolin-4-yl)-2,3,4a,8a-tetrahydro-1H-quinolin-4-one as yellowish solid (yield 40%, content 91%); MS-FAB (M+H+)=402.0; Rf (polar method): 2.20 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09006255B2 |
| Source dataset | uspto-grants-2015_04 |
| ORD ID | ord-3293087f03c74bfb8cc8fc4a8b45d050 |
| Source note | uspto-grants-2015_04 |