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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 391328Generated: October 29, 2026

P,P-Diphenylphosphinic azide → 4-(5-(1-Aminocyclopropyl)pyridin-3-yl)-2-chlorobenzonitrile

https://huagongshe.com/reaction/391328

Reaction equation

Participants

RoleNameHCIDCharge
ReactantP,P-Diphenylphosphinic azideHCID 199401—
ReactantPotassium tert-butoxideHCID 23665647—
Reactant1-(5-(3-Chloro-4-cyanophenyl)pyridin-3-yl)cyclopropanecarboxylic acidHCID 59578410—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product4-(5-(1-Aminocyclopropyl)pyridin-3-yl)-2-chlorobenzonitrileHCID 59578418—

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of 1-(5-(3-chloro-4-cyanophenyl)pyridin-3-yl)cyclopropanecarboxylic acid (900 mg, 3.01 mmol) in toluene (50 mL) was added TEA (0.63 mL, 4.52 mmol) and diphenylphosphoryl azide (0.977 mL, 4.52 mmol), and the mixture was heated to 100° C. for 4 h. The mixture was then cooled to room temperature and concentrated in vacuo. The residue was re-dissolved in THF (100 mL) and a solution of KOtBu (2.03 g, 18.08 mmol) in THF (40 mL) was added. The mixture was stirred at 0° C. for 1 h. The mixture was then warmed to room temperature overnight. Silica gel (10 g) was added and the mixture was concentrated in vacuo. The residue was purified by silica chromatography eluting with a 0-10% MeOH-DCM gradient to give 4-(5-(1-aminocyclopropyl)pyridin-3-yl)-2-chlorobenzonitrile. m/z 270.0, 272.0 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383827B2
Source datasetuspto-grants-2013_02
ORD IDord-a69c51cb2fee4dffa9c7aac9d27013a5
Source noteuspto-grants-2013_02