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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 919615Generated: October 31, 2026

tert-butyl 4-methylpyridin-3-ylcarbamate → HCID 45092184, compound

https://huagongshe.com/reaction/919615

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-butyl 4-methylpyridin-3-ylcarbamateHCID 11063649—
CatalystAdams' catalystHCID 345198—
SolventAcetic AcidHCID 176—
ProductHCID 45092184HCID 4509218477.8%

Reaction Steps

Tert-butyl 4-methylpyridin-3-ylcarbamate (200 mg, 0.96 mmol) was dissolved in glacial acetic acid (5 mL) and treated with PtO2 (200 mg, 1:1 w/w) under an atmosphere of hydrogen. The reaction mixture was stirred at rt for 15 h. The reaction mixture was then filtered through a pad of Celite. The filtrate was neutralized with solid NaHCO3, and extracted with EtOAc (5×50 mL). The organic layer was dried over Na2SO4, concentrated in vacuo to yield the titled compound (160 mg, 77%), which was used for next step without further purification. 1H NMR (400 MHz, CDCl3): δ 4.38-4.21 (m, 1H), 3.32-2.81 (m, 3H), 2.63-2.49 (m, 2H), 2.41-2.32 (m, 1H), 1.78-1.56 (m, 3H), 1.59 (s, 9H), 1.05 and 0.98 (2d, J=6.8 Hz, 3H). ES-MS: m/z [M+1]=215.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09273028B2
Source datasetuspto-grants-2016_03
ORD IDord-b640654f644d46f2871b382be1680138
Source noteuspto-grants-2016_03