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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256234Generated: November 1, 2026

Trifluoroacetic acid → HCID 178524087, compound

https://huagongshe.com/reaction/1256234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 67494358HCID 67494358—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
ProductHCID 178524087HCID 17852408784.4%

Reaction Steps

A 250 ml round-bottomed flask is charged with 1.46 g of 5-(2,6-difluorophenyl)-1-(dimethylsulphamoyl)-1H-pyrazolo[4,3-c]isoquinoline-7-carboxylic acid in 100 ml of DCM and then 20 ml of TFA are added. The mixture is stirred at RT for 16 h. It is concentrated under RP and the solid obtained is taken up in 30 ml of saturated aqueous NaHCO3 solution and extracted with three times 30 ml of AcOEt. The aqueous phase is acidified to a pH of 1 by addition of 37% HCl and extracted with AcOEt. The organic phase is washed with saturated NaCl solution, dried over MgSO4, filtered and concentrated under RP to give 927 mg of 5-(2,6-difluorophenyl)-2H-pyrazolo[4,3-c]isoquinoline-7-carboxylic acid (beige solid), LC-MS-DAD-ELSD: 326(+)=(M+H)(+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461175B2
Source datasetuspto-grants-2013_06
ORD IDord-9fc60dcee1034aed8c5e5cc9d0f109f3
Source noteuspto-grants-2013_06