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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1907147Generated: October 30, 2026

7-[2-(3-chloro-pyridin-2-yl)-5-methoxy-2H-pyrazol-3-yl]-2-(4-methoxy-benzyl)-5-methyl-2H-8-oxa-1,2,6-triaza-cyclopenta[a]naphthalen-9-one → 6-{[2-(3-chloro-pyridin-2-yl)-5-methoxy-2H-pyrazole-3-carbonyl]-amino}-2-(4-methoxy-benzyl)-5-methyl-2H-indazole-7-carboxylic acid isopropyl amide

https://huagongshe.com/reaction/1907147

Reaction equation

Participants

RoleNameHCIDCharge
Reactant7-[2-(3-chloro-pyridin-2-yl)-5-methoxy-2H-pyrazol-3-yl]-2-(4-methoxy-benzyl)-5-methyl-2H-8-oxa-1,2,6-triaza-cyclopenta[a]naphthalen-9-oneHCID 58500462—
CatalystIsopropylamineHCID 6363—
SolventTetrahydrofuranHCID 8028—
Product6-{[2-(3-chloro-pyridin-2-yl)-5-methoxy-2H-pyrazole-3-carbonyl]-amino}-2-(4-methoxy-benzyl)-5-methyl-2H-indazole-7-carboxylic acid isopropyl amideHCID 58500455—

Reaction Conditions

Temperature20 °C

Reaction Steps

A solution of 7-[2-(3-chloro-pyridin-2-yl)-5-methoxy-2H-pyrazol-3-yl]-2-(4-methoxy-benzyl)-5-methyl-2H-8-oxa-1,2,6-triaza-cyclopenta[a]naphthalen-9-one (0.100 g, 0.189 mmol) in tetrahydrofurane (2 ml) was treated with 16 drops of isopropyl amine and stirred at 20° C. for three hours. The reaction mixture was evaporated and the crude product was purified by flash chromatography on silica gel using a mixture of 75% ethyl acetate 25% cyclohexane. The desired product showed the physical data reported in the corresponding table (P.34.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08598078B2
Source datasetuspto-grants-2013_12
ORD IDord-1f87041f4a054198808f8a7f123c1b28
Source noteuspto-grants-2013_12