HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triphenylphosphine → 4-Methylsulphanyl-7-(4-morpholinobut-2-en-1-yloxy)quinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | ethyl N-ethoxycarbonyliminocarbamate | HCID 220568 | — |
| Reactant | 4-Morpholinobut-2-en-1-ol | HCID 53926128 | — |
| Reactant | 7-Hydroxy4-methylsulphanylquinazoline | HCID 135674019 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-Methylsulphanyl-7-(4-morpholinobut-2-en-1-yloxy)quinazoline | HCID 53697233 | 55.5% |
Reaction Steps
Using a procedure analogous to the one described for the synthesis of the starting material in Example 16, 4-morpholinobut-2-en-1-ol (1.27 g, 8.13 mmol), (J. Med. Chem. 1972, 15, 110-112), was reacted with 7-hydroxy-4-methylsulphanylquinazoline (1.2 g, 6.25 mmol), (prepared as described for the starting material in Example 8), in methylene chloride (30 ml) in the presence of triphenylphosphine (4.09 g, 1.56 mmol) and diethyl azodicarboxylate (2.46 ml, 1.56 mmol) to give 4-methylsulphanyl-7-(4-morpholinobut-2-en-1-yloxy)quinazoline (1.15 g, 55%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06294532B1 |
| Source dataset | uspto-grants-2001_09 |
| ORD ID | ord-7ea7870dcb114cb8a9db38d038fdd17f |
| Source note | uspto-grants-2001_09 |