HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526400Generated: October 25, 2026
Hydrochloric Acid → HCID 178509615, compound
https://huagongshe.com/reaction/526400
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-Hydrazinonicotinic acid | HCID 3782617 | — |
| Reactant | Ethyl 2-(4-cyanophenyl)-3-(dimethylamino)acrylate | HCID 117601544 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Product | HCID 178509615 | HCID 178509615 | 77% |
Reaction Steps
Combined 6-hydrazinylnicotinic acid (6.00 g, 39.2 mmol) and ethyl 2-(4-cyanophenyl)-3-(dimethylamino)acrylate (10.05 g, 41.1 mmol) and 2-propanol (80 mL) and treated with 1.85% hydrochloric acid (77 mL, 39.2 mmol). The reaction was stirred at room temperature for 16 h, then Hunig's base (34.1 mL, 196 mmol) was add to the suspension which became homogeneous. The mixture was stirred for 3 h. The reaction mixture was washed with isopropyl acetate (2×150 mL). The combined organic layers were extracted with water (40 mL) and the combined aqueous layers were concentrated in vacuo to give a solid. The solid was triturated with 1N HCl (300 mL), filtered and washed with water (20 mL), then slurried in ethanol (350 mL) and granulated overnight. The solid was collected by filtration and dried in vacuum to give the title compound (9.20 g, 77% yield) as a tan solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 7.79 (d, J=8.34 Hz, 2H) 8.14 (br. s., 2H) 8.47 (d, J=7.07 Hz, 1H) 8.71 (br. s., 2H) 8.97 (s, 1H) 13.44 (br. s., 1H) 13.60 (br. s., 1H). MS [M+H]307.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09345713B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-e26f3241a5404f938c8c11f6afc299c8 |
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| Source note | uspto-grants-2016_05 |
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