HuagongsheHuagongshe Chemistry Print Report · For research reference only
Propargyl alcohol → 4-(Methylthio)-6-methoxy-7-(3-hydroxyprop-1-ynyl)quinazoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Propargyl alcohol | HCID 7859 | — |
| Reactant | 4-(Methylthio)-6-methoxy-7-(trifluoromethanesulphonyloxy)quinazoline | HCID 86761099 | — |
| Catalyst | Triethylamine | HCID 8471 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(Methylthio)-6-methoxy-7-(3-hydroxyprop-1-ynyl)quinazoline | HCID 68677156 | 17% |
Reaction Steps
4-(methylthio)-6-methoxy-7-(trifluoromethanesulphonyloxy)quinazoline (1.0 g, 2.82 mmol) in dimethylformamide (30 ml) was reacted with propargyl alcohol (0.51 ml, 8.75 mmol) in the presence of bisdichloro(triphenylphosphine) palladium (100 mg, 0.14 mmol) copper (I) iodide (40 mg) and triethylamine (1.7 ml, 0.0124 mmol) at 90° C. for 2.5 hours under argon. The solvent was evaporated in vacuo, water and hydrochloric acid (2.0 N) were added, and the mixture was extracted with ethyl acetate. Purification by flash chromatography on silica gel, eluting with 7.5% methanol in dichloromethane, yielded 4-(methylthio)-6-methoxy-7-(3-hydroxyprop-1-ynyl)quinazoline (122 mg, 17% yield):
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07709479B1 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-42c6ac856b084e63aa63b595414e1d06 |
| Source note | uspto-grants-2010_05 |