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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 571308Generated: November 1, 2026

Trifluoroacetic acid → HCID 86681716, compound

https://huagongshe.com/reaction/571308

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86681715HCID 86681715—
SolventDichloromethaneHCID 6344—
ProductHCID 86681716HCID 8668171697%

Reaction Steps

To a solution of tert-butyl 2-(5-(N-(2-(4-methylpiperazin-1-yl)ethyl)methylsulfonamido)-1,3-dioxoisoindolin-2-yl)acetate (140 mg, 0.291 mmol) in dry DCM (4 ml) cooled to 0° C., TFA (0.449 ml, 5.83 mmol) was added, and the mixture was stirred at room temperature for 24 hours. The volatiles were removed under vacuum and the crude residue was dried affording 2-(5-(N-(2-(4-methylpiperazin-1-yl)ethyl)methylsulfonamido)-1,3-dioxoisoindolin-2-yl)acetic acid 2,2,2-trifluoroacetic acid salt (152 mg, 0.282 mmol, 97% yield, MS/ESI+ 424.8 [MH]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09024027B2
Source datasetuspto-grants-2015_05
ORD IDord-e3c1581ed37c4f568dc4da40ddfb43ff
Source noteuspto-grants-2015_05