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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 585462Generated: October 30, 2026

Ethanolamine → [(2-{[(1R)-1-Phenyl-1,2-dihydro[1,4]oxazino[2,3,4-jk]carbazol-7-yl]oxy}ethyl)amino]ethanol

https://huagongshe.com/reaction/585462

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
ReactantSodium IodideHCID 5238—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloroethyl (1R) 1-phenyl-1,2-dihydro[1,4]oxazino[2,3,4-jk]carbazol-7-yl etherHCID 12148639—
SolventDimethylformamideHCID 6228—
Product[(2-{[(1R)-1-Phenyl-1,2-dihydro[1,4]oxazino[2,3,4-jk]carbazol-7-yl]oxy}ethyl)amino]ethanolHCID 6979623924%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a mixture of 2-chloroethyl (1R)-1-phenyl-1,2-dihydro[1,4]oxazino[2,3,4-jk]carbazol-7-yl ether in DMF (20 mL) is added sodium iodide (1.0 g, 6.7 mmol), potassium carbonate (2.0 g, 14.5 mmol), and ethanolamine (0.42 mL, 7.0 mmol). The mixture is heated to 85° C. for 18 h. The mixture then is partitioned between water and CH2Cl2. The layers are separated and the organic layer washed twice with water (200 mL). The organic layer is dried over anhydrous sodium sulfate, filtered and concentrated. Column chromatography with silica gel (60 mL) using CH3OH/CH2Cl2 (2/98) and then rechromatographed with CH3OH/CH2Cl2/NH4OH (4/96/0.1) gave 0.62 g (24%) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06932961B1
Source datasetuspto-grants-2005_08
ORD IDord-2385cd9ba68540e5af294e76add1d989
Source noteuspto-grants-2005_08