HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butylamine → 3-(Butylamino)-N-methyl-4-nitrobenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butylamine | HCID 8007 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 21884189 | HCID 21884189 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(Butylamino)-N-methyl-4-nitrobenzamide | HCID 21884179 | — |
Reaction Steps
To a solution of N-methyl-3-fluoro-4-nitrobenzamide (300 mg, 1.64 mmol) and diisopropylethylamine (0.43 mL, 2.46 mmol) in DMF (7 mL) was added butylamine (0.203 mL, 2.05 mmol) and the solution was stirred at room temperature overnight. The solution was concentrated, the residue dissolved in ethyl acetate and washed with 1 N HCl. The organic phase was dried over MgSO4 and concentrated to give N-methyl-3-butylamino-4-nitrobenzamide as a yellow oil that was used without further purification (380 mg, 92%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07138420B2 |
| Source dataset | uspto-grants-2006_11 |
| ORD ID | ord-fb3f97fd64f8451f8176831643e18526 |
| Source note | uspto-grants-2006_11 |