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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2194644Generated: October 30, 2026

4-Aminotricyclo[3.3.1.13,7]decane-1-methanol → 3-{2-[1-(3-Hydroxy-2,2-dimethyl-propionyl)-piperidin-4-yl]-ethoxy}-N-(5-hydroxymethyl-adamantan-2-yl)-benzamide

https://huagongshe.com/reaction/2194644

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Aminotricyclo[3.3.1.13,7]decane-1-methanolHCID 57928167—
Reactant3-{2-[1-(3-Hydroxy-2,2-dimethyl-propionyl)-piperidin-4-yl]-ethoxy}-benzoic acidHCID 68782049—
Product3-{2-[1-(3-Hydroxy-2,2-dimethyl-propionyl)-piperidin-4-yl]-ethoxy}-N-(5-hydroxymethyl-adamantan-2-yl)-benzamideHCID 25108993—

Reaction Steps

Prepared from 3-{2-[1-(3-hydroxy-2,2-dimethyl-propionyl)-piperidin-4-yl]-ethoxy}-benzoic acid and 4-amino-1-hydroxymethyladamantane to give the title compound as a mixture of two isomers. 1H NMR (400 MHz, CDCl3) δ: 7.31-7.38 (m, 2H), 7.24-7.29 (m, 1H), 7.02 (d, 1H), 6.31-6.43 (m, 1H), 4.33-4.45 (m, 2H), 4.17-4.24 (m, 1H), 4.07 (t, 2H), 3.49 (s, 2H), 3.26 (d, 2H), 2.74-2.87 (m, 2H), 2.12-2.19 (m, 2H), 2.01-2.05 (m, 1H), 1.42-1.93 (m, 15H), 1.27 (s, 6H), 1.14-1.23 (m, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08334305B2
Source datasetuspto-grants-2012_12
ORD IDord-6426d9f98ee14ba28bd0c1a27c9fe0d5
Source noteuspto-grants-2012_12