HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1668950Generated: October 29, 2026
3-(Trifluoromethyl)aniline → 6-bromo-7-methyl-8-nitro-N-(3-(trifluoromethyl)phenyl)quinazolin-4-amine
https://huagongshe.com/reaction/1668950
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-(Trifluoromethyl)aniline | HCID 7375 | — |
| Reactant | 6-Bromo-4-chloro-7-methyl-8-nitroquinazoline | HCID 58942247 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | 6-bromo-7-methyl-8-nitro-N-(3-(trifluoromethyl)phenyl)quinazolin-4-amine | HCID 67338629 | 48% |
Reaction Steps
To a microwave vial were added 3-(trifluoromethyl)aniline (343 μl, 2777 μmol), 6-bromo-4-chloro-7-methyl-8-nitroquinazoline (840 mg, 2777 μmol) and IPA (5 mL). The reaction mixture was heated to 140° C. for 20 min. On cooling a ppt was observed to form which was then washed with hexane, filtered and air-dried to afford 6-bromo-7-methyl-8-nitro-N-(3-(trifluoromethyl)phenyl)quinazolin-4-amine (569 mg, 48.0% yield) as an amorphous yellow solid. MS (M+H)+ 427, 429.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07989461B2 |
|---|
| Source dataset | uspto-grants-2011_08 |
|---|
| ORD ID | ord-72f93c4e0b0c4cd29bef5868eedf52ef |
|---|
| Source note | uspto-grants-2011_08 |
|---|