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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 715487Generated: October 26, 2026

4-chloro-2-(1-(5-methyl-6-(2,2,2-trifluoroethoxy)pyridin-3-yl)ethyl)-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-1-one → HCID 178425440, compound

https://huagongshe.com/reaction/715487

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-chloro-2-(1-(5-methyl-6-(2,2,2-trifluoroethoxy)pyridin-3-yl)ethyl)-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-1-oneHCID 89874936—
Reactant1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazole-3-carboxamideHCID 89875477—
SolventTrifluoroacetic acid methylene chlorideHCID 21863450—
ProductHCID 178425440HCID 17842544011%

Reaction Steps

The reaction is carried out in a similar manner to Example-1 (Method-A) using 4-chloro-2-(1-(5-methyl-6-(2,2,2-trifluoroethoxy)pyridin-3-yl)ethyl)-2,3-dihydro-1H-pyrrolo[3,4-c]pyridin-1-one (50 mg, 0.13 mmol, Intermediate-2, single enantiomer) and 1-((2-(trimethylsilyl)ethoxy)methyl)-1H-pyrazole-3-carboxamide (63 mg, 0.26 mmol). The obtained crude is diluted with DCM/TFA (1:1, 2 mL), and the mixture is stirred at rt for 1 h. Then, the solvent is removed in vacuo, and the residue is purified by preparative LC-MS to give 6.3 mg (11% yield) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09187475B2
Source datasetuspto-grants-2015_11
ORD IDord-9bc4006b347e482fa8871624be5051ab
Source noteuspto-grants-2015_11