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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 85451Generated: October 28, 2026

3-(Aminomethyl)-6-methyl-4-propylpyridin-2(1H)-oneacetate → HCID 54596997, compound

https://huagongshe.com/reaction/85451

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(Aminomethyl)-6-methyl-4-propylpyridin-2(1H)-oneacetateHCID 67124140—
Reactant6-(4-((dimethylamino)methyl)piperidin-1-yl)-1-isopropyl-1H-indazole-4-carboxylic acidHCID 67468401—
ProductHCID 54596997HCID 54596997—

Reaction Steps

The title compound was prepared using the procedure described for example 37 (step c) from 6-(4-((dimethylamino)methyl)piperidin-1-yl)-1-isopropyl-1H-indazole-4-carboxylic acid and 3-(aminomethyl)-6-methyl-4-propyl-2(1H)-pyridinone. 1H NMR (400 MHz, DMSO-d6) δ ppm 0.89 (t, J=7.33 Hz, 3H), 1.14-1.32 (m, 2H), 1.42 (m, 6H), 1.45-1.55 (m, 2H), 1.57-1.68 (m, 1H), 1.72-1.89 (m, 3H), 2.03-2.21 (m, 12H), 2.63-2.79 (m, 2H), 3.54-3.66 (m, 1H), 3.81 (m, 2H), 4.37 (d, J=4.80 Hz, 2H), 4.94 (quin, J=6.63 Hz, 1H), 5.91 (s, 1H), 7.05 (s, 1H), 7.32 (d, J=1.77 Hz, 1H), 8.14 (s, 1H), 8.44 (t, J=5.05 Hz, 2H) 11.24-11.80 (m, 1H); LCMS: (M+H)+=507.1

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846935B2
Source datasetuspto-grants-2014_09
ORD IDord-99e3dfa5b891453baa7beb382e1659f0
Source noteuspto-grants-2014_09