HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1350094Generated: November 2, 2026
2,4-Difluoroaniline → HCID 17954364, compound
https://huagongshe.com/reaction/1350094
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Difluoroaniline | HCID 9709 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N-Benzyl-2-chloroacetamide | HCID 96233 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 17954364 | HCID 17954364 | — |
Reaction Steps
A mixture of N-benzyl-2-chloroacetamide (700 mg—obtained as described for intermediate 1), DIPEA (0.76 mL) and 2,4-difluoro-aniline (0.4 mL) in anhydrous DMF (5 mL) was stirred at 100° C. for 40 hours under a Nitrogen atmosphere. Then, more DIPEA (0.2 mL) was added and the mixture was heated to 100° C. for further 4 hours. After cooling to room temperature, the solution was diluted with AcOEt and washed with water and ice. The separated aqueous phase was extracted with further AcOEt (3×20 mL). The combined organic extracts were dried and concentrated in vacuo. The residue was purified by flash chromatography (CH/AcOEt 7:3) to give the title compound (600 mg) as a beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07214680B2 |
|---|
| Source dataset | uspto-grants-2007_05 |
|---|
| ORD ID | ord-f244d97d7b12416f95d805c3d542f455 |
|---|
| Source note | uspto-grants-2007_05 |
|---|