HuagongsheHuagongshe Chemistry Print Report · For research reference only
3-Bromoaniline → N-(3-Bromophenyl)-6-nitroquinazolin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 3-Bromoaniline | HCID 11562 | — |
| Reactant | 4-Chloro-6-nitroquinazoline | HCID 11356257 | — |
| Product | N-(3-Bromophenyl)-6-nitroquinazolin-4-amine | HCID 5328041 | — |
Reaction Steps
3-Bromoaniline is coupled with 4-chloro-6-nitroquinazoline, to produce 4-[(3-bromophenyl)amino]-6-nitroquinazoline, which is reduced thereafter to the corresponding 6-aminoquinazoline. The 4-[(3-bromophenyl)amino]-6-aminoquinazoline is then reacted with bistributyltin, using tetrakis(triphenylphosphine)palladium in triethylamine solution as the reaction catalyst. The stanylated quinazoline is then reacted with bromine-76 or bromine-77, in the presence of an oxidizing agent, to produce bromine-76 labeled or bromine-77 labeled 4-[(3-bromophenyl)amino]-6-aminoquinazoline, which is further reacted with acryloyl chloride as described, to yield the final bromine-76 labeled or bromine-77 labeled product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06562319B2 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-78d4083cde6e430184da2e6362e6b1b5 |
| Source note | uspto-grants-2003_05 |