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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094039Generated: October 29, 2026

1,3-Dichloroacetone → HCID 178423966, compound

https://huagongshe.com/reaction/1094039

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-DichloroacetoneHCID 10793—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Amino-6-(trifluoromethyl)pyridineHCID 821024—
Reactant1-Methyl-4-phenyl-1,3-dihydroimidazole-2-thioneHCID 20146433—
SolventDimethylformamideHCID 6228—
Solvent1,2-DimethoxyethaneHCID 8071—
ProductHCID 178423966HCID 178423966—

Reaction Steps

1,3-dichloroacetone (0.01 mL, 0.11 mmol) was added dropwise to a solution of 6-trifluoromethyl-pyridin-2-ylamine (0.016 g, 0.10 mmol) in 1,2-dimethoxyethane (1.0 mL), and the mixture was left to stir at room temperature for 2 h. The solvent was removed in vacuo and the resulting residue re-dissolved in ethanol (1.0 mL). The reaction mixture was subsequently heated under reflux for 2 h, and the solvent was removed under reduced pressure. DIPEA (0.05 mL, 0.25 mmol) and 1-methyl-4 phenyl-1,3-dihydro-imidazole-2-thione (0.017 g, 0.09 mmol) were sequentially added to a solution of the crude product in DMF (1.0 mL). The reaction mixture was then heated at 60° C. for 2 h after which LC-MS showed complete consumption of the starting materials. The solvent was removed under reduced pressure and the crude product purified using preparative LC-MS to yield the title compound. LC-MS: m/z=389.1 (MH+), tR=0.52 min, method C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08133897B2
Source datasetuspto-grants-2012_03
ORD IDord-fe5699911c3540b384882c9eabf4a6b4
Source noteuspto-grants-2012_03