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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1641209Generated: October 26, 2026

N-(2-Aminoethyl)piperidine → 3-Fluoro-5-piperidin-1-yl-N-[4-({2-[(2-piperidin-1-ylethyl)amino]pyrimidin-4-yl}oxy)-1-naphthyl]benzamide

https://huagongshe.com/reaction/1641209

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-(2-Aminoethyl)piperidineHCID 33944—
Reactant3-fluoro-N-[4-(2-methanesulfonyl-pyrimidin-4-yloxy)-naphthalen-1-yl]-5-piperidin-1-yl-benzamideHCID 66737969—
Product3-Fluoro-5-piperidin-1-yl-N-[4-({2-[(2-piperidin-1-ylethyl)amino]pyrimidin-4-yl}oxy)-1-naphthyl]benzamideHCID 59553210—

Reaction Steps

Compound is prepared from 3-fluoro-N-[4-(2-methanesulfonyl-pyrimidin-4-yloxy)-naphthalen-1-yl]-5-piperidin-1-yl-benzamide and 2-piperidin-1-yl-ethylamine according to conditions described in general procedure C. Mp: 88-89° C.; 1H NMR (400 MHz, DMSO-d6) δ 1.31-1.39 (m, 6 H), 1.58-1.61 (m, 6 H), 1.99-2.27 (m, 6H), 2.90-3.24 (m, 2 H), 3.23-3.29 (m, 4 H), 6.20-6.31 (bd, 1 H), 6.90-6.98 (m, 2 H), 7.15 (d, J =8.8 Hz, 1 H), 7.37 (d, J=8.0 Hz, 1 H), 7.43 (s, 1 H), 7.50-7.62 (m, 3 H), 7.78-7.80 (m, 1 H), 7.96 (d, J=8.0 Hz, 1 H), 8.20 (s 1 H), 10.40 (s, 1 H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08114873B2
Source datasetuspto-grants-2012_02
ORD IDord-4b043934a2dd4f389de416e1156b60c6
Source noteuspto-grants-2012_02