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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2305622Generated: November 1, 2026

4-Methylmorpholine → Methyl-4-{5-[2-(2-anilino-1,3-benzoxazol6-yl)-acetylamino]-2-methoxyphenoxy}-3-methyl-butanoate

https://huagongshe.com/reaction/2305622

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant2-Phenylaminobenzoxazol-6-acetic acidHCID 11149837—
ReactantMethyl 2-methyl-3-(2-methoxy-5-aminophenoxy)butyrateHCID 53892958—
ReactantHCID 178418300HCID 178418300—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductMethyl-4-{5-[2-(2-anilino-1,3-benzoxazol6-yl)-acetylamino]-2-methoxyphenoxy}-3-methyl-butanoateHCID 54563344—

Reaction Steps

To a mixture of 2-phenylaminobenzoxazole-6-acetic acid(0.067 g), methyl 2-methyl-3-(2-methoxy-5-aminophenoxy)butyrate(0.057 g), hydroxybenzotriazole (0.067 g), and N-methylmorpholine(0.05 ml) in dimethylformamide(0.25 ml) was added 1-(3-dimethylaminopropyl)3-ethylcarbodiimide hydrochloride(0.095 g). The resultant mixture was stirred for 48 hrs then added to water and extracted with ethyl acetate. The organic layer was separated, washed with aqueous acetic acid, brine, aqueous sodium bicarbonate (2 times), dried and evaporated to dryness. The residue was purified by purified by chromatography on silica using an increasingly polar mixture of ethyl acetateldichloromethane and the appropriate fraction yielded, after evaporation to dryness, a solid which was triturated with a mixture of diethylether/hexane to give the product (0.08 g) as a purple-pink solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06441012B1
Source datasetuspto-grants-2002_08
ORD IDord-40cbb133dd7a46b0b2b9a6dc9d61c7f1
Source noteuspto-grants-2002_08