HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aniline → 2-morpholin-4-ylmethyl-6-nitro-N-phenyl-benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aniline | HCID 6115 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Morpholin-4-ylmethyl-6-nitro-benzoic acid | HCID 59841069 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 2-morpholin-4-ylmethyl-6-nitro-N-phenyl-benzamide | HCID 59841084 | — |
Reaction Steps
A solution of compound 6 (0.62 g, 2.3 mmol) in THF (50 mL) was treated with thionyl chloride (0.94 mL), stirred at room temperature for 4 h, and evaporated to dryness. The residue was dissolved in THF (50 mL) and treated with aniline (0.58 mL, 6.4 mmol) and diisopropylethylamine (1.12 mL, 6.4 mmol). The reaction mixture was stirred for 4 h, concentrated, dissolved in dichloromethane (50 mL), washed with saturated aqueous sodium bicarbonate (0.25 mL) and brine (25 mL), dried with sodium sulfate, and concentrated. The crude residue of compound 7 then was purified by flash chromatography (5% methanol in dichloromethane).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09149477B2 |
| Source dataset | uspto-grants-2015_10 |
| ORD ID | ord-4cb5685c7d704101a33d27a42d8c5284 |
| Source note | uspto-grants-2015_10 |