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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1424498Generated: November 2, 2026

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

https://huagongshe.com/reaction/1424498

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant1-Cyclopropyl-1,3-dihydroimidazo[4,5-c]pyridine-2-oneHCID 22349361—
ReactantN-carboxylatoiminocarbamateHCID 51573101—
Reactant(1-(4,4-difluorobutyl)-1H-imidazo[4,5-b]pyridin-2-yl)methanolHCID 67991781—
SolventTetrahydrofuranHCID 8028—
Product1-cyclopropyl-3-((1-(4,4-difluorobutyl)-1H-imidazo[4,5-b]pyridin-2-yl)methyl)-1H-imidazo[4,5-c]pyridin-2(3H)-oneHCID 6797586859.4%

Reaction Steps

To a suspension of (1-(4,4-difluorobutyl)-1H-imidazo[4,5-b]pyridin-2-yl)methanol 43-5 (470 mg, 1.9 mmol), 1-cyclopropyl-1H-imidazo[4,5-c]pyridin-2(3H)-one 10-d (431 mg, 2.3 mmol) and triphenylphosphine (613 mg, 2.3 mmol) in 14 ml dry THF was added (E)-diïsopropyl diazene-1,2-dicarboxylate (0.6 ml, 2.9 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 (450 mg, 58%). m/z=399 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08927720B2
Source datasetuspto-grants-2015_01
ORD IDord-afe3384bdf39444eafa93b06fc7d9cbc
Source noteuspto-grants-2015_01