HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 4-Chloro-7-methoxy-6-(3-(4-morpholinyl)propoxy)quinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 4-Chloro-6-(3-chloropropoxy)-7-methoxyquinazoline | HCID 50742264 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Chloro-7-methoxy-6-(3-(4-morpholinyl)propoxy)quinazoline | HCID 22649221 | 85% |
Reaction Steps
DMF (3 lt), 6-(3-chloropropoxy)-7-methoxy-4-chloro quinazoline (200 gm) and morpholine (210 gm), were heated to 70-75° C. for 6-8 hours. The reaction mass was cooled to room temperature, and methylene chloride (2.5 lt) and water (2.5 lt) were charged. The layers separated and the aqueous layer extracted with methylene chloride twice (500 ml). The combined methylene chloride layer was washed with water, dried over sodium sulphate (10 gm) and concentrated completely at 35-40° C. to yield the title compound (200 gm, 85% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08350029B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-fe7033e0683c4b5ab74d31380884b9c7 |
| Source note | uspto-grants-2013_01 |