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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1171285Generated: October 27, 2026

Piperidine → 3-Fluoro-5-morpholin-4-yl-N-{4-[(2-piperidin-1-ylpyrimidin-4-yl)oxy]-1-naphthyl}benzamide

https://huagongshe.com/reaction/1171285

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
Reactant3-fluoro-N-(4-{[2-(methylsulfonyl)pyrimidin-4-yl]oxy}-1-naphthyl)-5-morpholin-4-ylbenzamideHCID 59553095—
Product3-Fluoro-5-morpholin-4-yl-N-{4-[(2-piperidin-1-ylpyrimidin-4-yl)oxy]-1-naphthyl}benzamideHCID 59553276—

Reaction Steps

Compound is prepared from 3-fluoro-N-(4-{[2-(methylsulfonyl)pyrimidin-4-yl]oxy}-1-naphthyl)-5-morpholin-4-ylbenzamide and piperidine according to conditions described in general procedure C. Mp: 190-191° C.; 1H NMR (400 MHz, CDCl3) δ 1.52-1.63 (m, 6 H), 3.27-3.63 (m, 4 H), 3.72 (m, 4 H), 3.87 (m, 4 H), 5.81-5.83 (m, 1 H), 5.92-5.94 (m, 1 H), 6.78 (d, J=10.0 Hz, 1 H), 7.08 (d, J=6.4 Hz, 1 H), 7.33-7.35 (m, 2 H), 7.50-7.61 (m, 2 H), 7.89-7.91 (m, 1 H), 7.96-8.14 (m, 1 H), 8.12-8.17 (m, 2 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07829560B2
Source datasetuspto-grants-2010_11
ORD IDord-a6a456a6a51a43a7864f8c70eb5f9069
Source noteuspto-grants-2010_11