HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl bromide → HCID 67024036, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl bromide | HCID 7841 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 67024027 | HCID 67024027 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67024036 | HCID 67024036 | 11.3% |
Reaction Steps
4-Isopropyl-N-(2-aminomethyl-indan-4-yl)-benzenesulfonamide (80 mg, 0.23 mmol), allyl bromide (30 mg, 0.23 mmol) and triethylamine (20 mg, 0.23 mmol) were dissolved in 2 mL of DMF and stirred at room temperature for 18 h. The solution was concentrated, water added and extracted with ethyl acetate. The organic phase was dried over MgSO4, filtered and the filtrate was evaporated in vacuo to give a residue which was purified by column chromatography using (dichloromethane-MeOH, 0-5%) to give a yellow oil (10 mg, 6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08486984B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-efb7ddbb0aae49fa95ab355fca95bee6 |
| Source note | uspto-grants-2013_07 |