HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 336339Generated: October 26, 2026
Water → Ethyl 2-((diphenylmethylene)amino)-2-(pyrazin-2-yl)acetate
https://huagongshe.com/reaction/336339
Participants
| Role | Name | HCID | Charge |
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| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ethyl 2-(diphenylmethyleneamino)acetate | HCID 319508 | — |
| Reactant | 2-Bromopyrazine | HCID 642800 | — |
| Catalyst | Tetrabutylammonium Iodide | HCID 67553 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | Ethyl 2-((diphenylmethylene)amino)-2-(pyrazin-2-yl)acetate | HCID 10246971 | — |
Reaction Steps
A mixture of ethyl 2-((diphenylmethylene)amino)acetate (6.0 g, 22.47 mmol), 2-bromopyrazine (7.1 g, 44.90 mmol), potassium carbonate (9.30 g, 67.40 mmol) and tetrabutyl ammonium iodide (8.10 g, 22.40 mmol) in N-methyl-2-pyrrolidone (25 mL) was heated in a sealed tube at 110° C. for 16 hours. The mixture was poured into water (100 mL) and extracted with ethyl acetate (3×50 mL). The organic layers were washed with brine (25 mL) and dried over sodium sulfate. Removal of solvent under vacuum afforded crude product which was purified in Combi-Flash instrument using a gradient of methanol in chloroform. Yield: 4.90 g (63%). 1H NMR (300 MHz, DMSO-d6) δ: 1.16 (t, 3H), 4.07 (q, 2H), 5.26 (s, 1H), 7.18 (dd, 2H), 7.38-7.61 (m, 8H), 8.56 (d, 1H), 8.57 (d, 1H), 8.60 (s, 1H). MS (ES) MH+: 346.3 for C21H19N3O2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889671B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-3c5640f5596048ceb5e6ad6d3633d084 |
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| Source note | uspto-grants-2014_11 |
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