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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718Generated: October 28, 2026

tert-Butyl carbamate → tert-Butyl (5-fluoro-6-methylpyridin-2-yl)carbamate

https://huagongshe.com/reaction/718

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butyl carbamateHCID 77922—
Reactant6-Chloro-3-fluoro-2-methylpyridineHCID 19867376—
ReagentPotassium Phosphate, TribasicHCID 62657—
Catalyst1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
Producttert-Butyl (5-fluoro-6-methylpyridin-2-yl)carbamateHCID 921331040%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 6-chloro-3-fluoro-2-methylpyridine (500 mg, 3.43 mmol), tert- Butyl carbamate (523 mg, 4.47 mmol), Potassium phosphate (1094 mg, 5.15 mmol), 9,9-Dimethyl-4,5-bis(diphenylphosphino)xanthene (99 mg, 0.17 mmol) and Tris(dibenzylideneacetone)dipalladium(0) (79 mg, 0.09 mmol) were combined in a sealed vial which was purged with nitrogen. Degassed toluene (5 mL) and water (5.00 mL) were added and the mixture was stirred under a nitrogen atmosphere at 90 °C for 6h. The reaction mixture was diluted with EtOAc and washed with saturated NaHCO3 solution, brine, dried over sodium sulfate, filtered and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel, eluting with mixtures of 5-50%EtOAc in heptane. Many spots isolated, but none of them seemed to be the desired product. Not continued.

Provenance & Evidence

Source dataset750 AstraZeneca ELN dataset
ORD IDord-849a1d763cb042f7907069ab25fe470c
Source note750 AstraZeneca ELN dataset