Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12119Generated: October 29, 2026

Ethanolamine → 8-{2-[2-(2-chloro-4-fluorophenyl)-1,1-dimethylethylamino]-1-hydroxyethyl}-6-hydroxy-4H-benzo[1,4]oxazin-3-one

https://huagongshe.com/reaction/12119

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolamineHCID 700—
ReactantBoron tribromideHCID 25134—
ReactantLithium borohydrideHCID 4148881—
ReactantHCID 22063474HCID 22063474—
ReactantHCID 22063496HCID 22063496—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product8-{2-[2-(2-chloro-4-fluorophenyl)-1,1-dimethylethylamino]-1-hydroxyethyl}-6-hydroxy-4H-benzo[1,4]oxazin-3-oneHCID 11502407—

Reaction Conditions

Temperature-78 °C

Reaction Steps

357 mg (1 mmol) of 6-benzyloxy-8-(2-ethoxy-2-hydroxyacetyl)-4H-benzo[1,4]oxazin-3-one and 202 mg (1 mmol) of 2-(2-chloro-4-fluorophenyl)-1,1-dimethylethylamine are reacted with lithium borohydride analogously to the method for Example 10(d). To debenzylate the ethanolamine thus obtained, it is dissolved in 3 mL of dichloromethane and cooled to −78° C. At this temperature, 2 mL of a 1 molar solution of boron tribromide in dichloromethane is added and the mixture is slowly allowed to come up to ambient temperature. The reaction mixture is combined with 10 mL dichloromethane and 3 mL water and filtered through an EXTRELUT® column. The eluate is freed from solvent and the residue is purified by chromatography. White solid. Yield: 70 mg (13%, trifluoroethyl acetate); mass spectroscopy: [M+H]+=409/11.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07727984B2
Source datasetuspto-grants-2010_06
ORD IDord-68992909e6e54c8bb9f71e7686ac5303
Source noteuspto-grants-2010_06