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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 85514Generated: October 27, 2026

6-Bromo-1-isopropyl-1H-indazole-4-carboxylic acid → 6-bromo-N-((4-(sec-butyl)-6-methyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-1-isopropyl 1H-indazole-4-carboxamide

https://huagongshe.com/reaction/85514

Reaction equation

Participants

RoleNameHCIDCharge
Reactant6-Bromo-1-isopropyl-1H-indazole-4-carboxylic acidHCID 67465443—
Reactant3-(aminomethyl)-4-(sec-butyl)-6-methylpyridin-2(1H)-oneHCID 67467859—
Product6-bromo-N-((4-(sec-butyl)-6-methyl-2-oxo-1,2-dihydropyridin-3-yl)methyl)-1-isopropyl 1H-indazole-4-carboxamideHCID 54596628—

Reaction Steps

The title compound was prepared in the same manner as described for example 3 (step c) from 6-bromo-1-(1-methylethyl)-1H-indazole-4-carboxylic acid (0.50 g, 1.77 mmol) and 3-(aminomethyl)-4-(sec-butyl)-6-methylpyridin-2(1H)-one (0.446 g, 2.296 mmol). The product was collected as 0.81 g (98%). 1H NMR (400 MHz, DMSO-d6) δ ppm 11.53 (s, 1H), 8.62 (t, J=4.7 Hz, 1H), 8.37 (s, 1H), 8.20 (s, 1H), 7.70 (d, J=1.5 Hz, 1H), 5.96 (s, 1H), 5.05 (quin, J=6.6 Hz, 1H), 4.41 (d, J=4.3 Hz, 2H), 2.95 (q, J=7.1 Hz, 1H), 2.15 (s, 3H), 1.48 (m, 8H), 1.07 (d, J=6.6 Hz, 3H), 0.74 (t, J=7.3 Hz, 3H). LC-MS(ES) [M+H]+ 459.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846935B2
Source datasetuspto-grants-2014_09
ORD IDord-54dff8cef13e495dbefcff6fe729726f
Source noteuspto-grants-2014_09