Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1660978Generated: October 31, 2026

3-tert-butyl-1-(4-methylphenyl)-1H-pyrazol-5-amine → N-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-2-(4-imidazo[4,5-b]pyridine-3-yl-phenyl)-acetamide

https://huagongshe.com/reaction/1660978

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-tert-butyl-1-(4-methylphenyl)-1H-pyrazol-5-amineHCID 2974132—
Reactant(4-Imidazo[4,5-b]pyridin-3-yl-phenyl)-acetic acidHCID 53213084—
ProductN-(5-tert-Butyl-2-p-tolyl-2H-pyrazol-3-yl)-2-(4-imidazo[4,5-b]pyridine-3-yl-phenyl)-acetamideHCID 11993382—

Reaction Steps

The title compound is prepared as described in Example 1 but using (4-imidazo[4,5-b]pyridin-3-yl-phenyl)-acetic acid (Step 7.1) and 5-tert-butyl-2-p-tolyl-2H-pyrazol-3-ylamine (see J. Med. Chem. 45, 2994-3008 (2002)). Title compound: ES-MS: 465.5 [M+H]+; 1H NMR (CDCl3) 8.55 (d, J=3.9 Hz, 1H), 8.38 (s, 1H), 8.24 (d, J=8.2 Hz), 7.83 (d, J=8.2 Hz, 2H), 7.52-7.48 (m, 1H), 7.45 (d, J=8.2 Hz, 2H), 7.42-7.40 (m, 1H), 7.39 (s, 1H, NH), 7.16 (d, J=8.2 Hz, 2H), 7.13 (d, J=8.2 Hz, 2H), 6.66 (s, 1H), 3.81 (s, 2H), 2.13 (s, 3H), 1.36 (s, 9H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08030311B2
Source datasetuspto-grants-2011_10
ORD IDord-230a25b9bd2848dcb7f7712e7fe85d82
Source noteuspto-grants-2011_10