HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 3-chloro-N-(2-morpholin-4-ylethyl)-4-nitro-benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Morpholinoethylamine | HCID 408285 | — |
| Reactant | 3-Chloro-4-nitrobenzoyl chloride | HCID 19077614 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 3-chloro-N-(2-morpholin-4-ylethyl)-4-nitro-benzamide | HCID 68682056 | — |
Reaction Steps
3-chloro-4-nitro-benzoyl chloride (Intermediate 54; 1.1 g, 5.00 mmol) was dissolved in DCM (10 mL) and N,N-diisopropylethylamine (1.05 mL, 6.00 mmol) added. The mixture was cooled in an ice/water bath and 4-(2-aminoethyl)morpholine (Aldrich; 0.66 mL, 5.00 mmol) in DCM (5 mL) added dropwise. The mixture was allowed to warm to room temperature and stirred for 0.5 hr. The reaction mixture was washed with brine, 2N NaOH, dried (MgSO4) and concentrated. Column chromatography of the residue (2% MeoH/DCM) gave the title compound as a yellow solid. (1.2 g, 76%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07709471B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-3f315437d9a14764a797a75efcb37da4 |
| Source note | uspto-grants-2010_05 |