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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1397151Generated: October 26, 2026

4-Aminopyridine → 1-Cyclopropyl-3-[2-(pyridin-4-ylamino)pyrimidin-4-yl]propan-2-one

https://huagongshe.com/reaction/1397151

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-AminopyridineHCID 1727—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant1-Cyclopropyl-3-[2-(methylsulfinyl)pyrimidin-4-yl]propan-2-oneHCID 67983470—
SolventTetrahydrofuranHCID 8028—
Product1-Cyclopropyl-3-[2-(pyridin-4-ylamino)pyrimidin-4-yl]propan-2-oneHCID 6798382686.3%

Reaction Steps

To a solution of 4-aminopyridine (328 mg, 3.49 mmol) in THF (2.344 mL) cooled to −78° C. was added LHMDS (583 mg, 3.49 mmol). The reaction was warmed to rt and stirred for 15 minutes. The reaction was again cooled to −78° C. and 1-cyclopropyl-3-[2-(methylsulfinyl)pyrimidin-4-yl]propan-2-one (7) (277 mg, 1.162 mmol) was added as a solution in THF (2 mL). The reaction was warmed to rt and stirred for 1 hour. The reaction was quenched by slow addition of saturated ammonium chloride and the volatiles evaporated. The residue was then partitioned between water and DCM. The organic layer was washed with brine, dried with sodium sulfate, and concentrated in vacuo. The crude residue was purified by Biotage™ silica gel chromatography [2-10% MeOH in DCM with 1% triethylamine] to afford the desired product as a yellow oil (269 mg, 86%). MS (ES+): m/z=269.2 (100) [MH+2]. HPLC: tR=0.69 minute over 3 minutes. Purity: >95% [HPLC (LC/MS) at 220 nm].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901147B2
Source datasetuspto-grants-2014_12
ORD IDord-631cb69100b849b09b37452223bcebdc
Source noteuspto-grants-2014_12