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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393279Generated: October 27, 2026

Triphenylphosphine → ethyl 5-{4-[2-(11-ethyl-6,11-dihydro-5-methyl-6-oxo-5H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-8-yl)ethoxy]phenyl}-2-methyl-3-furanecarboxylate

https://huagongshe.com/reaction/393279

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant11-Ethyl-8-(2-hydroxyethyl)-5-methyl-5,11-dihydro-6h-dipyrido[3,2-b:2',3'-e][1,4]diazepin-6-oneHCID 470717—
ReactantDiisopropyl azodicarboxylateHCID 5363146—
ReactantEthyl 5-(4-hydroxyphenyl)-2-methyl-3-furanecarboxylateHCID 22648859—
SolventTetrahydrofuranHCID 8028—
Productethyl 5-{4-[2-(11-ethyl-6,11-dihydro-5-methyl-6-oxo-5H-dipyrido[3,2-b:2',3'-e][1,4]diazepin-8-yl)ethoxy]phenyl}-2-methyl-3-furanecarboxylateHCID 2264886948.6%

Reaction Conditions

Temperature25 °C

Reaction Steps

DIAD (60 μL, 0.31 mmol) was added dropwise to a solution of 11-ethyl-5,11-dihydro-8-(2-hydroxyethyl)-5-methyl-6H-dipyrido[3,2-b:2′,3′-e][1,4]diazepin-6-one (75.8 mg, 0.25 mmol), ethyl 5-(4-hydroxyphenyl)-2-methyl-3-furanecarboxylate (75 mg, 0.30 mmol) and PPh3 (80.0 mg, 0.30 mmol) in THF (3 mL) at 25° C. The reaction mixture was stirred at 25° C. for 48 h. The mixture was concentrated under reduced pressure. The residue was purified by flash chromatography (Hexane:EtOAc, 3:2) to give the title compound (64 mg, 48% yield) as yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06806265B2
Source datasetuspto-grants-2004_10
ORD IDord-6f6e163c957d42e781fc7f9f6833de3c
Source noteuspto-grants-2004_10