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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2241806Generated: November 1, 2026

Acetic Acid → HCID 24780524, compound

https://huagongshe.com/reaction/2241806

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 59203854HCID 59203854—
SolventWaterHCID 962—
ProductHCID 24780524HCID 24780524—
ProductHCID 24780654HCID 24780654—

Reaction Steps

N-(2-Hydroxy-4-methoxyphenyl)-6-(methylamino)nicotinamide (0.23 g, 0.84 mmol) was mixed with acetic acid (4 mL) and the reaction was run in a microwave reactor at 200° C. for 25 minutes. The reaction mixture was added to water and made basic with sodium bicarbonate (sat. aq.). The aqueous solution was extracted three times with diethyl ether and the combined organic layers were washed with brine, dried (MgSO4) and evaporated. The crude product was purified first by flash column chromatography (hexane/ethyl acetate-gradient; 30-50% ethyl acetate), followed by preparative HPLC, resulting in the isolation of N-[5-(6-methoxy-1,3-benzoxazol-2-yl)pyridin-2-yl]-N-methylacetamide (6 mg) as a minor product, together with the title compound (0.13 g) as a solid. 1H NMR (400 MHz, CHLOROFORM-d) δ ppm 8.90 (d, 1H) 8.23 (dd, 1H) 7.59 (d, 1H) 7.10 (d, 1H) 6.94 (dd, 1H) 6.52 (d, 1H) 5.26 (br. s, 1H) 3.89 (s, 3H) 2.82-3.16 (m, 3 H); MS m/z (M+H) 256.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07670591B2
Source datasetuspto-grants-2010_03
ORD IDord-90beea9831ab428ca9145dde2751b65d
Source noteuspto-grants-2010_03