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
In one particular, 3-bromoaniline is reacted with 4-chloro-6-nitroquinazoline to produce 4-[(3-bromophenyl)amino]-6-nitro quinazoline, which is reduced thereafter, by means of an ethanolic solution of hydrazine hydrate and Raney®Nickel, to the corresponding 6-aminoquinazoline. The 4-[(3-bromophenyl)amino]-6-aminoquinazoline is then reacted with bistributyltin in the presence of tetrakis(triphenylphosphine)palladium in triethylamine solution and the obtained stanylated product is reacted thereafter with bromine-76, as described hereinabove. The obtained bromine-76 labeled 4-[(3-bromophenyl)amino]-6-aminoquinazoline is then reacted with an acryloyl chloride to produce a bromine-76 labeled {4-[(3-bromophenyl)amino]quinazoline-6-yl}acrylamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06562319B2 |
| Source dataset | uspto-grants-2003_05 |
| ORD ID | ord-6806258138fb4f2ea611e84416c1ef35 |
| Source note | uspto-grants-2003_05 |