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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364378Generated: October 31, 2026

N-(2-aminoethyl)-N-methylmethanesulfonamide → 1-[2-(Dimethylamino)-2-oxoethyl]-7-[(4-fluorophenyl)methyl]-4-hydroxy-N-{2-[methyl(methylsulfonyl)amino]ethyl}-2-oxo-1,2-dihydro-1,5-naphthyridine-3-carboxamide

https://huagongshe.com/reaction/2364378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-aminoethyl)-N-methylmethanesulfonamideHCID 28707509—
ReactantHCID 58882926HCID 58882926—
Product1-[2-(Dimethylamino)-2-oxoethyl]-7-[(4-fluorophenyl)methyl]-4-hydroxy-N-{2-[methyl(methylsulfonyl)amino]ethyl}-2-oxo-1,2-dihydro-1,5-naphthyridine-3-carboxamideHCID 69480927—

Reaction Steps

This compound was prepared from ethyl 1-[2-(dimethylamino)-2-oxoethyl]-7-[(4-fluorophenyl)methyl]-4-hydroxy-2-oxo-1,2-dihydro-1,5-naphthyridine-3-carboxylate and N-(2-aminoethyl)-N-methylmethanesulfonamide employing methods similar to those described in Example 245 and was purified by reverse phase preparative HPLC (C-18 stationary phase; 10-100% CH3CN/water/0.1% formic acid mobile phase). The product was obtained as a cream-colored solid: 1H NMR (d6-DMSO) δ 10.20 (1H, br t, J=6 Hz), 8.51 (1H, s), 7.76 (1H, s), 7.31 (2H, dd, J=8.3, 6 Hz), 7.12 (2H, t, J=˜9 Hz), 5.12 (2H, s), 4.11 (2H, s), 3.55 (2H, q, J=6 Hz), 3.25 (2H, m), 3.12 (3H, s), 2.85 (3H, s), 2.81 (3H, s), 2.79 (3H, s); HRMS calcd for C24H28FN5O6+H+: 534.1823. Found: 534.1812.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691991B2
Source datasetuspto-grants-2014_04
ORD IDord-7b0e15eaab844aa18db7a52dc95150f1
Source noteuspto-grants-2014_04