HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 537896Generated: October 29, 2026
1,3-Dichloroacetone → HCID 178423966, compound
https://huagongshe.com/reaction/537896
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,3-Dichloroacetone | HCID 10793 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Amino-6-(trifluoromethyl)pyridine | HCID 821024 | — |
| Reactant | 1-Methyl-4-phenyl-1,3-dihydroimidazole-2-thione | HCID 20146433 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | 1,2-Dimethoxyethane | HCID 8071 | — |
| Product | HCID 178423966 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08865711B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-5f0d816630d14db78773a9469b467d23 |
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| Source note | uspto-grants-2014_10 |
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