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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1793059Generated: November 4, 2026

Hydrochloric Acid → 2-(4-ethyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-1-hydroxymethyl-ethoxy)-benzamide

https://huagongshe.com/reaction/1793059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN-(2,2-Dimethyl-[1,3]dioxan-5-yloxy)-2-(4-ethyl-2-fluoro-phenylamino)-3,4-difluoro-benzamideHCID 22025657—
SolventEthanolHCID 702—
Product2-(4-ethyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-1-hydroxymethyl-ethoxy)-benzamideHCID 1019403484.6%

Reaction Steps

To a stirring solution of the product of Example 33, Step C, N-(2,2-dimethyl-[1,3]dioxan-5-yloxy)-2-(4-ethyl-2-fluoro-phenylamino)-3,4-difluoro-benzamide (0.416 g, 0.980 mmol) in ethanol (5 mL) was added 1 molar aqueous hydrochloric acid solution (1 mL). After stirring for 1 hour at ambient temperature the reaction mixture was partitioned between ethyl acetate and water. The organic layer was washed twice with water and twice with brine. The organic layer was collected, dried over sodium sulfate, filtered and concentrated in vacuo. The affording foam was crystallized in ethyl acetate and heptane to afford 2-(4-ethyl-2-fluoro-phenylamino)-3,4-difluoro-N-(2-hydroxy-1-hydroxymethyl-ethoxy)-benzamide (0.318 g, 84.6%) as a white crystalline solid: m.p. 91–93° C.; 1NMR (400 MHz; CD3OD) δ 7.38 (1H, t, J=6.8 Hz), 6.85–6.96 (3H, m), 6.73–6.78 (1H, m), 3.86–3.82 (1 H), 3.64 (4H, d, J=4.9 Hz), 2.58 (2H, q, J=15.1, 7.6 Hz), 1.19 (3H, t, J=7.6 Hz); 19F-NMR (376 MHz; CD3OD) 8–132.4, −134.6, −147.2; MS(APCI+)=385; Anal.calcd/found for C18H19F3N2O4: C, 56.25/56.38; H, 4.98/4.81; N, 7.29/7.25.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07078438B2
Source datasetuspto-grants-2006_07
ORD IDord-a7104acbbd12461a8b874be5fbda6497
Source noteuspto-grants-2006_07