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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1098579Generated: November 2, 2026

HCID 66728944, compound → 5-(Propan-2-yl)pyridin-3-amine

https://huagongshe.com/reaction/1098579

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 66728944HCID 66728944—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
Product5-(Propan-2-yl)pyridin-3-amineHCID 59135276134.1%

Reaction Steps

To a solution of 5-(prop-1-en-2-yl)pyridin-3-amine (0.773 g, 2.48 mmol) in ethanol (8 mL) was added 10% Pd/C (0.132 g, 0.124 mmol) and the resulting suspension was stirred under a hydrogen atmosphere (1 atm) for 18 h. The reaction was filtered through Celite® and washed forward with EtOH. The filtrate was concentrated, diluted with EtOAc (30 mL) and washed with H2O (1×15 ml) and brine (1×15 ml). The aqueous phase was back-extracted with EtOAc (1×20 ml). The combined organic layers were dried (MgSO4) and concentrated to afford 5-isopropylpyridin-3-amine (0.453 g, 134%) as a light yellow oil. MS (ESI) m/z: 137.1 (M+H+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08143293B2
Source datasetuspto-grants-2012_03
ORD IDord-132e49140dad42fab7c464c6af402992
Source noteuspto-grants-2012_03