HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1442980Generated: October 31, 2026
Methanol → N-(3-chloro-4-fluorophenyl)-5,7-dimethoxyquinazolin-4-amine
https://huagongshe.com/reaction/1442980
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | N-(3-chloro-4-fluorophenyl)-5,7-difluoroquinazolin-4-amine | HCID 68676704 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N-(3-chloro-4-fluorophenyl)-5,7-dimethoxyquinazolin-4-amine | HCID 68675529 | 69% |
Reaction Steps
Methanol (6.5 ml) and potassium tert-butoxide (18 g) were added sequentially, each in one portion, to a mixture of N-(3-chloro-4-fluorophenyl)-5,7-difluoroquinazolin-4-amine (13.8 g) in THF (270 ml) at room temperature under a nitrogen atmosphere. The mixture was heated at 75° C. for 18 hours 30 minutes and then cooled to room temperature and concentrated in vacuo to leave a brown solid. The solid was cooled to 0° C. and cold water was added and then the precipitate was filtered and dried to leave N-(3-chloro-4-fluorophenyl)-5,7-dimethoxyquinazolin-4-amine as a light brown solid (10.4 g, 69%); Mass spectrum MH+ 334.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07659279B2 |
|---|
| Source dataset | uspto-grants-2010_02 |
|---|
| ORD ID | ord-e49ab3aeb59a44fc87b6ea50dee6105d |
|---|
| Source note | uspto-grants-2010_02 |
|---|