HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Fluoro-2-methylaniline → N-Benzyl-2-(4-fluoro-2-methyl-phenylamino)acetamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Fluoro-2-methylaniline | HCID 67982 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N-Benzyl-2-chloroacetamide | HCID 96233 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | N-Benzyl-2-(4-fluoro-2-methyl-phenylamino)acetamide | HCID 17954343 | — |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
A mixture of N-benzyl-2-chloroacetamide (17.8 g), DIPEA (19.5 mL) and 4-fluoro-2-methyl-aniline (10.6 mL) in anhydrous DMF (174 mL) was stirred at 100° C. for 40 hours under a Nitrogen atmosphere. After cooling to r.t., the dark solution was partitioned between AcOEt (200 mL) and water (200 mL). The separated aqueous phase was extracted with further AcOEt (3×200 mL). The combined organic extracts were washed with water (200 mL), dried and concentrated in vacuo. The residue was purified by flash chromatography (CH/AcOEt 2:8) to give a dark solid, which was triturated with CH to give the title compound as a beige solid (16.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07214680B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-32be2152ebde416aaec4707f2bd9919e |
| Source note | uspto-grants-2007_05 |