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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 85419Generated: October 26, 2026

3-(aminomethyl)-6-methyl-4-(phenylmethyl)-2(1H)-pyridinone → 6-bromo-1-(1-methylethyl)-N-{[6-methyl-2-oxo-4-(phenylmethyl)-1,2-dihydro-3-pyridinyl]methyl}-1H-indazole-4-carboxamide

https://huagongshe.com/reaction/85419

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(aminomethyl)-6-methyl-4-(phenylmethyl)-2(1H)-pyridinoneHCID 67463678—
Reactant6-Bromo-1-isopropyl-1H-indazole-4-carboxylic acidHCID 67465443—
Product6-bromo-1-(1-methylethyl)-N-{[6-methyl-2-oxo-4-(phenylmethyl)-1,2-dihydro-3-pyridinyl]methyl}-1H-indazole-4-carboxamideHCID 54596554—

Reaction Steps

The title compound was prepared in the same manner as described for the example 4 from 6-bromo-1-(1-methylethyl)-1H-indazole-4-carboxylic acid (100 mg, 0.353 mmol) and 3-(aminomethyl)-6-methyl-4-(phenylmethyl)-2(1H)-pyridinone (129 mg, 0.565 mmol), wherein the reaction stir time was 12 h. The product was collected as a white solid (130 mg, 71%). 1H NMR (400 MHz, DMSO-d6) ppm 11.61 (s, 1H), 8.69 (s, 1H), 8.35 (s, 1H), 8.20 (s, 1H), 7.66 (s, 1H), 7.17-7.26 (m, 6H), 5.81 (s, 1H), 5.04 (m, 2H), 4.42 (s, 2H), 3.96 (s, 2H), 2.10 (s, 3H), 1.45 (d, 6H); MS(ES) [M+H]+ 495.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846935B2
Source datasetuspto-grants-2014_09
ORD IDord-119e8ed3cc454181b548a342a6b08b4d
Source noteuspto-grants-2014_09