HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-tert-Butylbenzylamine → N-(4-t-butylbenzyl) 3-(3-fluoro-4-methanesulfonylaminophenyl)propionamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-tert-Butylbenzylamine | HCID 2735655 | — |
| Reactant | Methyl 3-(3-fluoro-4-methanesulfonylaminophenyl)propionate | HCID 59684482 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-(4-t-butylbenzyl) 3-(3-fluoro-4-methanesulfonylaminophenyl)propionamide | HCID 44574279 | 58% |
Reaction Steps
The compound 26-2 (30 mg) prepared in Step 2 was dissolved in toluene (4 ml) and to the solution was added 4-t-butylbenzylamine (150 μl), followed by refluxing for 3 hours. The resulting mixture was concentrated under reduced pressure and the obtained residue was chromatographed on silica gel column (ethyl acetate/hexane=1/1) to yield the compound 26-3 (28 mg, 58%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08071650B2 |
| Source dataset | uspto-grants-2011_12 |
| ORD ID | ord-81ad59e9b2904ed59f21a8a1c88c02df |
| Source note | uspto-grants-2011_12 |