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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 516Generated: October 23, 2026

tert-Butyl carbamate → tert-butyl N-(3-fluoro-5-methyl-2-pyridinyl)carbamate

https://huagongshe.com/en/reaction/516

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl carbamateHCID 77922—
Reactant2-Chloro-3-fluoro-5-methylpyridineHCID 13541365—
ReagentSodium HydroxideHCID 14798—
Catalyst1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
CatalystPalladium (II) acetateHCID 4144353—
Solvent1,4-DioxaneHCID 31275—
Producttert-butyl N-(3-fluoro-5-methyl-2-pyridinyl)carbamateHCID 9006479825.74%

Reaction Conditions

Temperature100 °C

Reaction Steps

diacetoxypalladium (15.42 mg, 0.07 mmol) and(9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (39.8 mg, 0.07 mmol) were added to a degassed mixture of 2-chloro-3-fluoro-5-methylpyridine (100 mg, 0.69 mmol), tert-butyl carbamate (105 mg, 0.89 mmol) and 2-chloro-3-fluoro-5-methylpyridine (100 mg, 0.69 mmol) in dioxane (10 mL) at 21°C. The resulting mixture was stirred at 100 °C for 2 hours.Cooled. Adsorbed onto silica. The crude product was purified by flash silica chromatography, elution gradient 10 to 30% DCM in heptane. Pure fractions were evaporated to dryness to afford tert-butyl 3-fluoro-5-methylpyridin-2-ylcarbamate (40.0 mg, 25.7 %) as a cream solid. not pure enough to register ..

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-fde5e0f95519439ca9660af435fc14a6
Source note750 AstraZeneca ELN dataset