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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1842708Generated: October 25, 2026

Water → N'-(5-chloro-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-yl)-4-methoxy-6-(5-methyl-2,5-diazaspiro[3.4]octan-2-yl)benzene-1,3-diamine

https://huagongshe.com/reaction/1842708

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantAmmonium ChlorideHCID 25517—
Reactant5-chloro-N-[2-methoxy-4-(5-methyl-2,5-diazaspiro[3.4]octan-2-yl)-5-nitrophenyl]-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-amineHCID 71240785—
CatalystIronHCID 23925—
SolventEthanolHCID 702—
ProductN'-(5-chloro-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-yl)-4-methoxy-6-(5-methyl-2,5-diazaspiro[3.4]octan-2-yl)benzene-1,3-diamineHCID 8667723934%

Reaction Steps

A mixture of 5-chloro-N-[2-methoxy-4-(5-methyl-2,5-diazaspiro[3.4]octan-2-yl)-5-nitrophenyl]-4-pyrazolo[1,5-a]pyridin-3-ylpyrimidin-2-amine (Intermediate 46, 95 mg, 0.18 mmol), iron (61 mg, 1.09 mmol) and NH4Cl (7.32 mg, 0.14 mmol) was heated at reflux in ethanol (10.5 mL) and water (3.5 mL) for 2 h. The mixture was cooled and filtered through diatomaceous earth (Celite™). The filtrate was concentrated in vacuo and the residue was dissolved in CH2Cl2. This solution was washed with brine, dried (Na2SO4) and concentrated in vacuo. Purification by FCC, eluting with 2-6% 7N methanolic ammonia in CH2Cl2 gave the title compound (30 mg, 34%) as a brown gum; m/z: ES+ MH+ 491.5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946235B2
Source datasetuspto-grants-2015_02
ORD IDord-0c40728fc4d8420eb125881a7589bdca
Source noteuspto-grants-2015_02