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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1480238Generated: November 2, 2026

Piperidinocarbonitrile → HCID 90203749, compound

https://huagongshe.com/reaction/1480238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidinocarbonitrileHCID 73736—
ReactantHCID 90203779HCID 90203779—
SolventEthyl AcetateHCID 8857—
ProductHCID 90203749HCID 9020374967%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of N-[(2Z)-2-amino-1-(cyclopropylmethyl)-2-hydroxyimino-1-methyl-ethyl]-5-cyclopropyl-4-(2,2,2-trifluoroethoxy)pyridine-2-carboxamide (example 165a, 30 mg, 74.9 μmol) in piperidine-1-carbonitrile (130 mg, 130 μl, 1.18 mmol) was heated at 130° C. in a sealed tube for 2 hours. The reaction mixture was cooled to room temperature and was diluted with ethyl acetate. The organic phase was washed with water. The organic phase was collected and the aqueous phase was back-extracted with ethyl acetate. Combined organic phases were dried over sodium sulfate and evaporated down to dryness. The crude material was purified by flash chromatography on silica eluting with a heptane/ethyl acetate gradient to yield the title compound (21 mg, 67%). MS (ESI, m/z): 426.6 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409866B2
Source datasetuspto-grants-2016_08
ORD IDord-1a21faf5753841f78dfcb7f28b246d6f
Source noteuspto-grants-2016_08