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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364354Generated: November 2, 2026

N-(2-aminoethyl)acetamide → N-[2-(acetylamino)ethyl]-1-ethyl-7-[(4-fluorophenyl)methyl]-4-hydroxy-2-oxo-1,2-dihydro-1,5-naphthyridine-3-carboxamide

https://huagongshe.com/reaction/2364354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-aminoethyl)acetamideHCID 66082—
ReactantHCID 69482004HCID 69482004—
ProductN-[2-(acetylamino)ethyl]-1-ethyl-7-[(4-fluorophenyl)methyl]-4-hydroxy-2-oxo-1,2-dihydro-1,5-naphthyridine-3-carboxamideHCID 6948272560.8%

Reaction Steps

In a similar manner to that described in example 196, from ethyl 1-ethyl-7-[(4-fluorophenyl)methyl]-4-hydroxy-2-oxo-1,2-dihydro-1,5-naphthyridine-3-carboxylate (30 mg, 0.081 mmol) and N-(2-aminoethyl)acetamide (66 mg, 0.648 mmol) was prepared N-[2-(acetylamino)ethyl]-1-ethyl-7-[(4-fluorophenyl)methyl]-4-hydroxy-2-oxo-1,2-dihydro-1,5-naphthyridine-3-carboxamide (21 mg, 60% yield) as a white solid after purification by reverse phase HPLC. 1H NMR (CDCl3) δ 10.31 (br s, 1 H), 8.49 (s, 1 H), 7.38 (s, 1 H), 7.14-7.11 (m, 2 H), 7.01-6.96 (m, 2 H), 6.85 (br s, 1 H), 4.16 (m, 2 H), 4.10 (s, 2 H), 3.54 (m, 2 H), 3.42 (m, 2 H), 1.94 (s, 3 H), 1.20 (m, 3 H); HRMS m/z calcd for C22H24FN4O4: 427.1776 Found: 427.1783.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691991B2
Source datasetuspto-grants-2014_04
ORD IDord-41897088552d4b408c3a0d03af902516
Source noteuspto-grants-2014_04