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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 922043Generated: October 31, 2026

Chloroacetone → HCID 67286623, compound

https://huagongshe.com/reaction/922043

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetoneHCID 6571—
ReactantSodium HydroxideHCID 14798—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 67287071HCID 67287071—
SolventEthyl AcetateHCID 8857—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 67286623HCID 6728662331.1%

Reaction Conditions

Temperature140 °C

Reaction Steps

To a solution of 150 mg (0.45 mmol) 2-ethylsulfanyl-N-[(3-fluorophenyl)-methyl]-6-(methyl-amino)-4-methyl-pyridine-3-carboxylic acid amide (synthesis is described in section a) of example 123) in NMP (1 ml) were added 229 μl (1.35 mmol) DIPEA and 39 μl (0.50 mmol) chloroacetone. The mixture was heated in the MW to 140° C. for 40 min and subsequently partiotionated between a 1M aq. NaOH sol and EtOAc. The organic layer was separated, washed with a 1M aq. NaOH sol, water and brine, dried over MgSO4 and concentrated in vacuo. Purification of the residue by CC (hexane/EtOAc 13:7) provided 53 mg (0.14 mmol, 30%) 2-Ethylsulfanyl-N-[(3-fluorophenyl)-methyl]-4-methyl-6-[methyl-(2-oxo-propyl)-amino]-pyridine-3-carboxylic acid amide (example 253). [M+H]+ 390.2

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278103B2
Source datasetuspto-grants-2016_03
ORD IDord-b241baea729e4c2198d8a55e0e3fdc56
Source noteuspto-grants-2016_03