HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Bromoaniline → HCID 19611610, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Bromoaniline | HCID 7807 | — |
| Reactant | 2-chloro-6,7-dimethylquinoxaline | HCID 825321 | — |
| Product | HCID 19611610 | HCID 19611610 | 37% |
Reaction Steps
A preferred method of synthesis of 2-(4-bromophenylamino)-6,7-quinoxaline (Compound 30) is as follows: 200 mg of 2-chloro-6,7-dimethyl quinoxaline (synthesized according to the protocol at Section 5.13, step 2) and 0.8 g of p-bromoaniline were heated at 100° for 3.5 hours. Chromatography gave 25 mg (37% yield) of a light yellow solid, having a melting point of 235° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05712395 |
| Source dataset | uspto-grants-1998_01 |
| ORD ID | ord-6ad68fa7d76f47f0b91fba515d1c6d38 |
| Source note | uspto-grants-1998_01 |