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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446514Generated: October 25, 2026

tert-Butyl (3-{[(2-fluoro-4-nitrophenyl)carbonyl](methyl)amino}propyl)methylcarbamate → tert-Butyl (3-{[(4-amino-2-fluorophenyl)carbonyl](methyl)amino}propyl)methylcarbamate

https://huagongshe.com/reaction/446514

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl (3-{[(2-fluoro-4-nitrophenyl)carbonyl](methyl)amino}propyl)methylcarbamateHCID 86663428—
ReactantHCID 178418361HCID 178418361—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
Producttert-Butyl (3-{[(4-amino-2-fluorophenyl)carbonyl](methyl)amino}propyl)methylcarbamateHCID 8666342995%

Reaction Steps

A solution of the compound (300 mg, 0.810 mmol) obtained in Example 12a in methanol (8 mL) was added to 10% palladium-carbon (dry; 30 mg), the atmosphere in the system was replaced with a hydrogen atmosphere, and then the mixture was stirred at room temperature for 30 minutes. The atmosphere in the system was replaced with a nitrogen atmosphere, then 10% palladium-carbon (dry; 90 mg) was further added, the atmosphere in the system was replaced with a hydrogen atmosphere, and the mixture was stirred at room temperature for 30 minutes. The atmosphere in the system was replaced with a nitrogen atmosphere, and then the mixture was filtered through celite. The solvent was evaporated under reduced pressure to give the title compound (260 mg; yield, 95%) as a light brown oily substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08476253B2
Source datasetuspto-grants-2013_07
ORD IDord-366f45b8d13345d5b47c808e72686a7f
Source noteuspto-grants-2013_07