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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600682Generated: October 29, 2026

7-amino-4-fluoro-2-methyl-2H-indazole → 2-[(2-Bromo-pyridin-4-ylmethyl)-amino]-N-(4-fluoro-2-methyl-2H-indazol-7-yl)-benzamide

https://huagongshe.com/reaction/600682

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-amino-4-fluoro-2-methyl-2H-indazoleHCID 23118988—
ReactantMethyl 2-{[(2-bromopyridin-4-yl)methyl]amino}benzoateHCID 58763671—
Product2-[(2-Bromo-pyridin-4-ylmethyl)-amino]-N-(4-fluoro-2-methyl-2H-indazol-7-yl)-benzamideHCID 23118982—

Reaction Steps

2-[(2-Bromo-pyridin-4-ylmethyl)-amino]-N-(4-fluoro-2-methyl-2H-indazol-7-yl)-benzamide was prepared from 2-[(2-bromo-pyridin-4-ylmethyl)-amino]-benzoic acid methyl ester and 7-amino-4-fluoro-2-methyl-2H-indazole in analogy to the procedures detailed in Example 4A; 1H-NMR (300 MHz, d6-DMSO) 9.86 (1H, s), 8.60 (1H, s), 8.32 (1H, d), 8.13 (1H, t), 7.83 (1H, d), 7.58-7.61 (2H, m), 7.42 (1H, d), 7.30 (1H, t), 6.82 (1H, dd), 6.72 (1H, t), 6.59 (1H, d), 4.52 (2H, d), 4.22 (3H, s); m/z (ES+) 454, 456 [M+H, Br isotopes]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902229B2
Source datasetuspto-grants-2011_03
ORD IDord-e4f496a24f9a40d284fc7f1762662bce
Source noteuspto-grants-2011_03