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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 706552Generated: October 29, 2026

2-Morpholinoethanol → N-(1-((6-cyclopropylpyridin-2-yl)methyl)-3-methyl-1H-indazol-4-yl)-7-(2-(4-isopropylpiperazin-1-yl)ethoxy)imidazo[1,2-a]pyridine-3-carboxamide

https://huagongshe.com/reaction/706552

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-MorpholinoethanolHCID 61163—
Reactant7-fluoro-N-(1-((6-isopropylpyridin-2-yl)methyl)-3-methyl-1H-indazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamideHCID 67976063—
ProductN-(1-((6-cyclopropylpyridin-2-yl)methyl)-3-methyl-1H-indazol-4-yl)-7-(2-(4-isopropylpiperazin-1-yl)ethoxy)imidazo[1,2-a]pyridine-3-carboxamideHCID 5738433648%

Reaction Steps

Prepared according Example 1, Step B, substituting N-(1-((6-cyclopropylpyridin-2-yl)methyl)-3-methyl-1H-indazol-4-yl)-7-fluoroimidazo[1,2-a]pyridine-3-carboxamide for 7-fluoro-N-(1-((6-isopropylpyridin-2-yl)methyl)-3-methyl-1H-indazol-4-yl)imidazo[1,2-a]pyridine-3-carboxamide and substituting 2-(4-isopropylpiperazin-1-yl)ethanol for 2-morpholinoethanol to give the title compound (48%). MS (APCI), positive scan, m/z=593.8 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174981B2
Source datasetuspto-grants-2015_11
ORD IDord-610027a95d1c4a46a8c0f58b87feb45c
Source noteuspto-grants-2015_11