HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(3-Chloro-4-fluorophenyl)-7-methoxy-6-nitroquinazolin-4-amine → N4-(3-Chloro-4-fluorophenyl)-7-methoxy-4,6-quinazolinediamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(3-Chloro-4-fluorophenyl)-7-methoxy-6-nitroquinazolin-4-amine | HCID 21847811 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | N4-(3-Chloro-4-fluorophenyl)-7-methoxy-4,6-quinazolinediamine | HCID 21847826 | 99% |
Reaction Steps
7.1 g of (3-Chloro-4-fluoro-phenyl)-(7-methoxy-6-nitro-quinazolin-4-yl)-amine was reduced using Raney nickel catalyst in THF, then filtered and evaporated to give 6.4 g N4-(3-Chloro-4-fluoro-phenyl)-7-methoxy-quinazoline-4,6-diamine (99% yield). This product was reacted with 4-Chloro-but-2-enoyl chloride as described in Scheme 1 to provide 4-Chloro-but-2-enoic acid [4-(3-chloro-4-fluoro-phenylamino)-7-methoxy-quinazolin-6-yl]-amide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07772243B2 |
| Source dataset | uspto-grants-2010_08 |
| ORD ID | ord-6fce9690bdba4702add5b871463c9db1 |
| Source note | uspto-grants-2010_08 |