Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | HCID 10582773 | HCID 10582773 | — |
| Reactant | 2,5,6-Trichloropyridine-3-carboxamide | HCID 53750930 | — |
| Reactant | HCID 178418922 | HCID 178418922 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 86661723 | HCID 86661723 | 87.4% |
Reaction Steps
A mixture of compound 2,5,6-trichloronicotinamide (0.6 g, 2.7 mmol), 1-(3-hydroxypropyl)cyclopropanol (370 mg, 3.2 mmol) and tert-BuOK (363 mg, 3.2 mmol) in DMF was stirred at room temperature overnight and the reaction mixture was then poured into cold water, the mixture was extracted twice with ethyl acetate, the combined organic layers were washed with brine twice, dried over Na2SO4 and concentrated, the residue was purified by column chromatography (silica gel, Petroleum ether: EtOAc=1:0 to 5:1) to give the 5,6-dichloro-2-(3-(1-hydroxycyclopropyl)propoxy)nicotinamide (0.72 g, 73%). 1H-NMR (400 MHz, DMSO-d6) δ (ppm) 8.65 (s, 1H), 8.29 (s, 1H), 8.03 (s, 1H), 5.48 (s, 1H), 4.82 (t, 2H, J=6.4 Hz), 2.36 (m, 2H), 1.97 (m, 2H), 0.94 (t, 2H), 0.73 (t, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09145429B2 |
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| Source dataset | uspto-grants-2015_09 |
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| ORD ID | ord-d07dc308ae21410f9446de8e0e88d520 |
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| Source note | uspto-grants-2015_09 |
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