Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 6-hydrazinyl-N-((tetrahydro-2H-pyran-4-yl)methyl)nicotinamide | HCID 63705793 | — |
| Reactant | ethyl 3-(dimethylamino)-2-(4-oxopyridin-1(4H)-yl)acrylate | HCID 131732877 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 178523066 | HCID 178523066 | 26.6% |
Reaction Steps
Combined 6-hydrazinyl-N-((tetrahydro-2H-pyran-4-yl)methyl)nicotinamide, 1.0 HCl (30 mg, 0.105 mmol), ethyl 3-(dimethylamino)-2-(4-oxopyridin-1(4H)-yl)acrylate (37.1 mg, 0.157 mmol) and acetic acid (0.018 mL, 0.314 mmol) in 2-propanol (0.8 mL) and stirred at 20° C. for 1 hour and then at 50° C. for 16 hours and then 80° C. for 24 h. The reaction mixture was then diluted with 200 uL DMSO and purified by prep HPLC (ACN/water with formic acid) to give the title compound (11 mg, 26.6% yield) as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.11-1.32 (m, 2 H) 1.62 (d, J=13.4 Hz, 2 H) 1.73-1.90 (m, 1 H) 3.20 (t, J=6.2 Hz, 2 H) 3.25 (s, 2 H) 3.86 (dd, J=11.4, 2.8 Hz, 2 H) 6.56 (br. s., 2 H) 8.19 (br. s., 2 H) 8.40 (t, J=7.7 Hz, 3 H) 8.71 (t, J=5.3 Hz, 1 H) 8.91 (s, 1 H). MS m/z 396 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040522B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-36cfc6cbfd5044b7a416d45bef3f8b78 |
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| Source note | uspto-grants-2015_05 |
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