HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1779117Generated: November 3, 2026
Diisopropylethylamine → HCID 86712743, compound
https://huagongshe.com/reaction/1779117
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2,4-Dichloro-5-(trifluoromethyl)pyrimidine | HCID 2782774 | — |
| Reactant | 1-(5-Aminopyridin-2-yl)ethan-1-one | HCID 21827816 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 86712743 | HCID 86712743 | 44.8% |
Reaction Steps
A suspension of 1-(5-aminopyridin-2-yl)ethanone (2.08 g, 15.3 mmol) in DMF (30 mL) and DIPEA (6.65 mL, 38.2 mmol) was stirred at room temperature for 15 minutes. 2,4-Dichloro-5-(trifluoromethyl)pyrimidine (2.47 mL, 18.33 mmol) was added in 4 portions over 5 minutes. The reaction mixture was stirred at 60° C. for 2 hours under a nitrogen atmosphere before it was diluted with water and EtOAc. The aqueous was extracted several times with EtOAc and the combined organic phases were washed with water, brine, dried (Na2SO4), filtered and the solvent evaporated in vacuo. The crude product was adsorbed onto silica gel and purified by column chromatography (CombiFlash Rf, 40 g SiO2 Cartridge, 0-30% EtOAc in cyclohexane) to give 2.17 g of a white solid. The 1:1 regiosiomeric mixture was dissolved in a minimum volume of cold (5° C.) acetonitrile (4-8 mL), sonicated for 10 seconds then filtered and dried to give the title compound (A141) as a white solid (1.14 g, 23%). LCMS-B: rt 7.34 min; m/z 317 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09266864B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-fc7c5d732afd43c1b41e872689e07d98 |
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| Source note | uspto-grants-2016_02 |
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