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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2264523Generated: October 26, 2026

Benzyl Alcohol → N-{4-[2-Amino-6-(benzyloxy)-3,5-dicyano-4-pyridinyl]phenyl}acetamide

https://huagongshe.com/reaction/2264523

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzyl AlcoholHCID 244—
ReactantPotassium CarbonateHCID 11430—
ReactantN-{4-[2-Amino-3,5-dicyano-6-(phenylsulphanyl)-4-pyridinyl]phenyl}acetamideHCID 12016387—
ProductN-{4-[2-Amino-6-(benzyloxy)-3,5-dicyano-4-pyridinyl]phenyl}acetamideHCID 10221564—

Reaction Conditions

Temperature100 °C

Reaction Steps

58 mg (0.15 mmol) of N-{4-[2-amino-3,5-dicyano-6-(phenylsulfanyl)-4-pyridinyl]phenyl}acetamide [prepared analogously to Kambe et al., Synthesis, 531-533 (1981)] are, together with 41 mg (0.3 mmol) of potassium carbonate, dissolved/suspended in 1.88 g (=1.8 ml, 17.4 mmol) of benzyl alcohol, and the mixture is stirred at 100° C. for 3.5 h. The benzyl alcohol is evaporated under reduced pressure and the evaporation residue is purified by preparative HPLC on reversed-phase silica gel (gradient: water/acetonitrile 90:1010:90 in 38 minutes).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07855219B2
Source datasetuspto-grants-2010_12
ORD IDord-6a6345a0e9c445b8ae3a4ec1262644f8
Source noteuspto-grants-2010_12