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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209083Generated: October 30, 2026

Trifluoroacetic acid → HCID 117842915, compound

https://huagongshe.com/reaction/2209083

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 117843316HCID 117843316—
SolventDichloromethaneHCID 6344—
ProductHCID 117842915HCID 117842915—

Reaction Steps

To the TFA salt of (R)-4-((R)-1-((1-cyclopropyl-5-(5-(piperazin-1-yl)pyridin-2-yl)-1H-benzo[d]imidazol-7-yl)oxy)ethyl)pyrrolidin-2-one: (45 mg, 0.1 mmol) in DCM (1 mL) and TEA (0.07 mL, 0.5 mmol) was added acetic anhydride (0.014 mL, 0.15 mmol). The reaction was stirred at rt for 2 h. The mixture was then concentrated and purified by prep-HPLC (MeCN:water gradient; TFA modified) to give (R)-4-((R)-1-((5-(5-(4-acetylpiperazin-1-yl)pyridin-2-yl)-1-cyclopropyl-1H-benzo[d]imidazol-7-yl)oxy)ethyl)pyrrolidin-2-one: 3.59 as a TFA salt. The salt was then converted to the free base by treatment with MP carbonate resin.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376441B2
Source datasetuspto-grants-2016_06
ORD IDord-497a152cdcff4d529e60436ca40f4e87
Source noteuspto-grants-2016_06