HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1364525Generated: October 29, 2026
Sodium Carbonate → N-(4-amino-5-cyano-6-phenylpyridin-2-yl)acetamide
https://huagongshe.com/reaction/1364525
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Phenyl dihydrogen orthoborate | HCID 78412 | — |
| Reactant | N-(4-Amino-6-bromo-5-cyano-pyridin-2-yl)-acetamide | HCID 11557905 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | water THF DMF | HCID 86606902 | — |
| Product | N-(4-amino-5-cyano-6-phenylpyridin-2-yl)acetamide | HCID 11658882 | 72.7% |
Reaction Steps
A mixture of bromide from Example 65A (45 mg, 0.18 mmol), Na2CO3 (38 mg, 0.35 mmol), and Pd(PPh3)4 (10 mg, 0.009 mmol) was stirred in DMF/THF/H2O (1:1:0.5) under nitrogen in a microwave reactor vial. Phenyl boric acid (26 mg, 0.21 mmol) was added. The resulting mixture was capped and heated at 130° C. for 20 min in a microwave reactor. The crude mixture was partitioned between EtOAc and water. The organic layer washed with water and brine, dried over Na2SO4, and evaporated under reduced pressure. The crude residue was purified by a Gilson reverse phase HPLC to provide the titled compound (33 mg, 72% yield). 1H NMR (300 MHz, d6-DMSO) δ 10.44 (s, 1H), 7.74-7.68 (m, 2H), 7.55 (s, 1H), 7.52-7.46 (m, 3H), 6.98 (s, 2H), 2.08 (s, 3H). MS (ESI) m/e 253 (M+H)+; m/e 251 (M−H)−.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07888374B2 |
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| Source dataset | uspto-grants-2011_02 |
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| ORD ID | ord-5fa09abe9e974bc0b543db820b30e33e |
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| Source note | uspto-grants-2011_02 |
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