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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1818738Generated: November 3, 2026

2,6-Lutidine → HCID 178461823, compound

https://huagongshe.com/reaction/1818738

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,6-LutidineHCID 7937—
ReactantTetrahydrofuranHCID 8028—
ReactantHCID 86611175HCID 86611175—
ReactantHCID 86611176HCID 86611176—
ProductHCID 178461823HCID 178461823—

Reaction Conditions

Temperature25 °C

Reaction Steps

The solution of {[2,4-bis-(2,4-difluoro-phenoxy)-pyrimidin-5-yl]-chloro-methyl}-(2-methanesulfonyl-1-methyl-ethylidene)-amine was added to a solution of BOC carbazate (766 g) and 2,6-lutidine (930 g) in tetrahydrofuran (2.0 liters) at 5° C. The reaction mixture was stirred at 25° C. for 24 hours. The reaction mixture was quenched with water (3.0 liters) diluted with methylene chloride (2.0 liters) and the reaction pH was adjusted to pH 3 by addition of 4N HCl (2.4 liters). The layers were separated and the organic layer was washed with saturated sodium bicarbonate (2.0 liters) and a 1:1 mixture of water and saturated brine. The organic layer was concentrated under reduced pressure for 12 hours to give N′-[[2,4-bis-(2,4-difluoro-phenoxy)-pyrimidin-5-yl]-((R)-2-methanesulfonyl-1-methyl-ethylamino)-methylene]-hydrazinecarboxylic acid tert-butyl ester (2.0 kg, quantitative) as a pale yellow powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07601726B2
Source datasetuspto-grants-2009_10
ORD IDord-c5853b0849134593b5869994306cba78
Source noteuspto-grants-2009_10