HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 178434265, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-Bromoethanol | HCID 10898 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 178434266 | HCID 178434266 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 178434265 | HCID 178434265 | 7.3% |
Reaction Steps
To a solution of 5-[(S)-3-benzylpiperazin-1-yl]-3-(3-methylindazol-5-yl)-[1,2,4]triazine 12 (28.5 mg, 0.074 mmol.) in acetonitrile (2 mL) was added sodium bicarbonate (6.2 mg, 0.074 mmol.) and 2-bromoethanol (9.2 mg, 0.11 mmol.). The reaction mixture was heated under gentle reflux overnight. Ethyl acetate (50 mL) was added. The organic layer was washed with water and brine. The organic layer was dried over sodium sulfate. The organic solvent was evaporated under reduced pressure. The crude product was purified by RP-HPLC to yield the desired 5-[(S)-3-benzyl-4-hydroxyethyl-piperazin-1-yl]-3-(3-methylindazol-5-yl)-[1,2,4]triazine 60 (2.3 mg, 0.0054 mmol.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07528132B2 |
| Source dataset | uspto-grants-2009_05 |
| ORD ID | ord-fb76d5a42b144ff3aa36cbd3e12496a3 |
| Source note | uspto-grants-2009_05 |