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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1020168Generated: October 30, 2026

Cyclopentanone → HCID 52917034, compound

https://huagongshe.com/reaction/1020168

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCyclopentanoneHCID 8452—
ReactantBorane;2-methylpyridineHCID 16217944—
Reactant5-Phenylethynyl-pyridin-2-ylamineHCID 46854190—
SolventAcetic acid methanolHCID 10129899—
ProductHCID 52917034HCID 52917034—

Reaction Conditions

Temperature40 °C

Reaction Steps

5-Phenylethynyl-pyridin-2-ylamine (100 mg, 0.515 mmol), cyclopentanone (77 mg, 0.927 mmol) and 2-picoline borane (85 mg, 0.927 mmol) were dissolved in 5.5 ml MeOH:AcOH (10:1 v/v) and stirred for 48 hours at 40° C. MeOH was then evaporated and the residue was acidified to pH 1 with 6 ml 10% HCl. The resulting white suspension was stirred for 2 hours. The mixture was extracted with dichloromethane and brine. The pH of the aqueous layer was adjusted to 12 by addition of conc. NaOH and the mixture was extracted twice with dichloromethane. The organic extracts were dried with sodium sulfate, filtered and evaporated. The crude product was purified by flash chromatography on silicagel (heptane/ethyl acetate 100:0→50:50 gradient). The desired compound was obtained as a light yellow solid (70 mg, 53%), MS: m/e=263.3 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08716316B2
Source datasetuspto-grants-2014_05
ORD IDord-d7c28bb2403c4c27b6bcd03ff776bb1a
Source noteuspto-grants-2014_05