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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716188Generated: October 31, 2026

HCID 71007327, compound → HCID 71007334, compound

https://huagongshe.com/reaction/716188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 71007327HCID 71007327—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductHCID 71007334HCID 71007334111.7%

Reaction Steps

tert-butyl (3-(3-aminopyridin-4-yl)-5-methylphenyl) carbamate. A solution of tert-butyl (3-methyl-5-(3-nitropyridin-4-yl)phenyl)carbamate (198 mg, 0.60 mmol) in EtOH (5 mL) and EtOAc (5 mL) was degassed by bubbling N2 (g) through the solution for 10 min. Pd/C (10 wt %, 64 mg, 0.060 mmol) was added. A gas bag with a 3-way stopcock filled with H2 was attached to the flask. The flask was evacuated under vacuum and then back-filled with H2 (3×). The mixture was stiffed overnight at RT. The solution was degassed by bubbling N2 (g) through the solution for 10 min and was then filtered through celite. The solution was concentrated to afford tert-butyl (3-(3-aminopyridin-4-yl)-5-methylphenyl)carbamate (200 mg, 0.67 mmol, 111% yield) as an off-white foam. MS (ESI, pos. ion) m/z: 300.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187486B2
Source datasetuspto-grants-2015_11
ORD IDord-886ab991c7fe4d059be079548838d921
Source noteuspto-grants-2015_11