HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 1-[2-(6-Chloro-hexyloxy)-benzyl]-4-(4-isopropyl-phenyl)-6-prop-2-ynyloxy-1H-quinazolin-2-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 1-Bromo-6-chlorohexane | HCID 80516 | — |
| Reactant | 1-(2-hydroxy-benzyl)-4-(4-isopropyl-phenyl)-6-prop-2-ynyloxy-1H-quinazolin-2-one | HCID 10224193 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 1-[2-(6-Chloro-hexyloxy)-benzyl]-4-(4-isopropyl-phenyl)-6-prop-2-ynyloxy-1H-quinazolin-2-one | HCID 60112826 | — |
Reaction Steps
To a solution of 482 mg (1.13 mmol) 1-(2-hydroxy-benzyl)-4-(4-isopropyl-phenyl)-6-prop-2-ynyloxy-1H-quinazolin-2-one in 2 ml dichloromethane is added 1 ml 1M aqueous NaOH. After stirring for 5 minutes the solvents are evaporated. The residue is dissolved in 4.8 ml DMEU and 0.25 ml (1.70 mmol) 1-bromo-6-chlorohexane are added. After stirring for 3 days at rt additional 0.083 ml 1-bromo-6-chlorohexane are added and stirring at rt is continued for 1 day. The reaction mixture is poured onto water, extracted with ethyl acetate and purified by flash chromatography (hexanes/ethyl acetate 6:1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08476286B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-2a5ae667d2b44d9fb2a80288d56c9c18 |
| Source note | uspto-grants-2013_07 |