HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1809128Generated: October 31, 2026
Potassium Iodide → 8-(5,6-dichloro-1H-benzimidazol-2-yl)-4-(2-morpholine-4-yl-ethyl)-3,4-dihydro-2H-benzo[1,4]oxazine
https://huagongshe.com/reaction/1809128
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(2-Chloroethyl)morpholine | HCID 76727 | — |
| Reactant | 8-(5,6-dichloro-1H-benzo[d]imidazol-2-yl)-3,4-dihydro-2H-benzo[b][1,4]oxazine | HCID 67094893 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 8-(5,6-dichloro-1H-benzimidazol-2-yl)-4-(2-morpholine-4-yl-ethyl)-3,4-dihydro-2H-benzo[1,4]oxazine | HCID 67094958 | 92.3% |
Reaction Steps
4.5 g (14 mmol) of 8-(5,6-dichloro-1H-benzo[d]imidazol-2-yl)-3,4-dihydro-2H-benzo[b][1,4]oxazine (compound 1a) obtained in Example 5 was dissolved in 100 mL of dimethylformamide. 1.3 g (7 mmol) of 4-(2-chloroethyl)morpholine, 0.58 g (3.5 mmol) of potassium iodide and 0.97 g (7 mmol) of K2CO3 were added thereto, followed by irradiation of microwave at 110° C. for 10 min. The reaction mixture was concentrated under reduced pressure, followed by dilution with ethyl acetate. The resulting product was washed with distilled water and saturated sodium chloride solution, followed by drying over magnesium sulfate and concentrating under reduced pressure. The resulting residue was subjected to column chromatography (ethyl acetate/hexane=1/1) to obtain the title compound (2.8 g, yield: 91%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08362012B2 |
|---|
| Source dataset | uspto-grants-2013_01 |
|---|
| ORD ID | ord-1d8e9a4c9c124238a505ae1c33f441b5 |
|---|
| Source note | uspto-grants-2013_01 |
|---|