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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantPhenyl dihydrogen orthoborateHCID 78412—
ReactantN-(4-Amino-6-bromo-5-cyano-pyridin-2-yl)-acetamideHCID 11557905—
CatalystHCID 178418397HCID 178418397—
Solventwater THF DMFHCID 86606902—
ProductN-(4-amino-5-cyano-6-phenylpyridin-2-yl)acetamideHCID 1165888272.7%

Reaction Conditions

Temperature130 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07888374B2
Source datasetuspto-grants-2011_02
ORD IDord-5fa09abe9e974bc0b543db820b30e33e
Source noteuspto-grants-2011_02