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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424496Generated: November 1, 2026

Triphenylphosphine → 1-cyclopropyl-3-((1-(4-fluorobutyl)-1H-imidazo[4,5-b]pyridin-2-yl)methyl)-1H-imidazo[4,5-c]pyridin-2(3H)-one

https://huagongshe.com/reaction/1424496

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant1-Cyclopropyl-1,3-dihydroimidazo[4,5-c]pyridine-2-oneHCID 22349361—
ReactantN-carboxylatoiminocarbamateHCID 51573101—
Reactant(1-(4-fluorobutyl)-1H-imidazo[4,5-b]pyridin-2-yl)methanolHCID 67991782—
SolventTetrahydrofuranHCID 8028—
Product1-cyclopropyl-3-((1-(4-fluorobutyl)-1H-imidazo[4,5-b]pyridin-2-yl)methyl)-1H-imidazo[4,5-c]pyridin-2(3H)-oneHCID 6797553263.3%

Reaction Steps

To a suspension of (1-(4-fluorobutyl)-1H-imidazo[4,5-b]pyridin-2-yl)methanol 42-5 (958 mg, 4.3 mmol), 1-cyclopropyl-1H-imidazo[4,5-c]pyridin-2(3H)-one 10-d (950 mg, 5.15 mmol) and triphenylphosphine (1350 mg, 5.15 mmol) in 30 ml dry THF was added (E)-diïsopropyl diazene-1,2-dicarboxylate (1.26 ml, 6.43 mmol) at room temperature. The reaction mixture was stirred at room temperature for 16 hours. The precipitate was filtered off and washed with some diethyl ether to obtain the title product as a white powder (1036 mg, 63%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927720B2
Source datasetuspto-grants-2015_01
ORD IDord-05dba1f719f54b228c812e8da763c73e
Source noteuspto-grants-2015_01