HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Hydrazino-3-(3-isopropoxy-phenyl)-3H-quinazolin-4-one → 4(3H)-Quinazolinone, 2-amino-3-[3-(1-methylethoxy)phenyl]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Hydrazino-3-(3-isopropoxy-phenyl)-3H-quinazolin-4-one | HCID 10614897 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | 4(3H)-Quinazolinone, 2-amino-3-[3-(1-methylethoxy)phenyl]- | HCID 10827705 | — |
Reaction Steps
A solution of 2-Hydrazino-3-(3-isopropoxy-phenyl)-3H-quinazolin-4-one (2.5g, 8.0 mmol) in 100 mL methanol-THF (1:1) was treated with Raney Ni (2.0), and resulting suspension was subjected to atmosphere of hydrogen at 52.0 psi for 30 hours with agitation at temperature of 50° C. An additional 1.0 g of Raney Ni was added and reaction was continued for additional 40 hours at 50° C. The mixture was then filtered through celite, and the solvent was removed in vacuo to give the title compound as a reddish yellow solid. This crude product was then titurated with ethyl acetate and hexane to isolate 1.85 g (78%) product as a light yellow solid, mp 130°-133° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05869665 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-ac755582ab2d4119bfda7bfda5dd3d48 |
| Source note | uspto-grants-1999_02 |