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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium IodideHCID 4875—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(2-Chloroethyl)morpholineHCID 76727—
Reactant8-(5,6-dichloro-1H-benzo[d]imidazol-2-yl)-3,4-dihydro-2H-benzo[b][1,4]oxazineHCID 67094893—
SolventDimethylformamideHCID 6228—
Product8-(5,6-dichloro-1H-benzimidazol-2-yl)-4-(2-morpholine-4-yl-ethyl)-3,4-dihydro-2H-benzo[1,4]oxazineHCID 6709495892.3%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08362012B2
Source datasetuspto-grants-2013_01
ORD IDord-1d8e9a4c9c124238a505ae1c33f441b5
Source noteuspto-grants-2013_01