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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 513966Generated: October 26, 2026

Ammonia → 2-(7-((3,4-Difluorobenzyl)oxy)-1,5-naphthyridin-3-yl)acetamide

https://huagongshe.com/reaction/513966

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantMethanolHCID 887—
ReactantEthyl 2-(7-((3,4-difluorobenzyl)oxy)-1,5-naphthyridin-3-yl)acetateHCID 90416945—
Product2-(7-((3,4-Difluorobenzyl)oxy)-1,5-naphthyridin-3-yl)acetamideHCID 86296849—

Reaction Steps

Ethyl 2-(7-((3,4-difluorobenzyl)oxy)-1,5-naphthyridin-3-yl)acetate (1.95 g, 5.44 mmol) was treated with a solution of ammonia in MeOH (7 M, 30 mL, 245 mmol). The slurry was stirred at ambient temperature for 30 h. The resulting precipitate was filtered and washed with MeOH to give the title compound as a cream colored solid. The crude product was azeotrope dried with toluene to remove traces of ammonia then dried on high vacuum for 48 h to give the title compound (1.79 g, 82%) as a pure white solid. 1H NMR (400 MHz, DMSO-d6) δ 8.81 (t, J=2.0 Hz, 2H), 8.21 (d, J=1.4 Hz, 1H), 7.88 (d, J=2.6 Hz, 1H), 7.75-7.58 (m, 2H), 7.50 (td, J=8.4, 10.7 Hz, 1H), 7.45-7.36 (m, 1H), 7.05 (br s, 1H), 5.34 (s, 2H), 3.66 (s, 2H). [M+H]=330.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09102674B2
Source datasetuspto-grants-2015_08
ORD IDord-86ed93e52a60475b8b6e95a3a7f4df2f
Source noteuspto-grants-2015_08