Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641156Generated: October 26, 2026

3-fluoro-N-(4-{[2-(methylsulfonyl)pyrimidin-4-yl]oxy}-1-naphthyl)-5-morpholin-4-ylbenzamide → N-[4-({2-[[amino(imino)methyl](methyl)amino]pyrimidin-4-yl}oxy)-1-naphthyl]-3-fluoro-5-morpholin-4-ylbenzamide

https://huagongshe.com/reaction/1641156

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-fluoro-N-(4-{[2-(methylsulfonyl)pyrimidin-4-yl]oxy}-1-naphthyl)-5-morpholin-4-ylbenzamideHCID 59553095—
ReactantHCID 178485088HCID 178485088—
ProductN-[4-({2-[[amino(imino)methyl](methyl)amino]pyrimidin-4-yl}oxy)-1-naphthyl]-3-fluoro-5-morpholin-4-ylbenzamideHCID 59553380—

Reaction Steps

Compound is prepared from 3-fluoro-N-(4-{[2-(methylsulfonyl)pyrimidin-4-yl]oxy}-1-naphthyl)-5-morpholin-4-ylbenzamide and N-methylguanidine according to conditions described in general procedure C. Mp: 155-157° C.; 1H NMR (400 MHz, DMSO-d6) δ 3.19-3.33(m, 7 H), 3.75-3.78(m, 4 H), 6.50(d, J=5.5 Hz, 1H), 7.04(d, J=12.0 Hz, 1 H), 7.27(d, J=9.1 Hz, 1 H), 7.34-7.68(m, 7 H), 7.80(d, J=8.8 Hz, 1H), 7.99(d, J=8.2 Hz, 1 H), 8.29(d, J=5.5 Hz, 1 H), 10.47(s, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114873B2
Source datasetuspto-grants-2012_02
ORD IDord-f5f5303085ad4b9abc95b857324a7245
Source noteuspto-grants-2012_02