Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | 5-Chloro-2-nitroaniline | HCID 74218 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Morpholino-2-nitroaniline | HCID 596725 | — |
Reaction Steps
Morpholine (1 equivalent) and 5-chloro-2-nitroaniline (1 equivalent) were dissolved in DMF, and TEA (2 equivalents) was added. The reaction mixture was heated at 120° C. overnight. The reaction mixture was then cooled to room temperature, most of the DMF was distilled off, and water was added to the residue to obtain the crude product as a precipitate. The solid was dried and purified by chromatography on silica gel (2-10% MeOH/CH2Cl2) to afford the desired product, 5-morpholin-4-yl-2-nitro-phenylamine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07825132B2 |
|---|
| Source dataset | uspto-grants-2010_11 |
|---|
| ORD ID | ord-e83079b7c1134ecaa06993039698bd7d |
|---|
| Source note | uspto-grants-2010_11 |
|---|