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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2209188Generated: October 31, 2026

Trifluoroacetic acid → HCID 117843592, compound

https://huagongshe.com/reaction/2209188

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantHCID 117843092HCID 117843092—
SolventDichloromethaneHCID 6344—
ProductHCID 117843592HCID 117843592—

Reaction Steps

The crude TFA salt of 4.27 (0.058 mmol) was suspended in DCM (1 mL) and Et3N (60 μL, 0.43 mmol) was added followed by acetic anhydride (6.5 μL, 0.069 mmol). The resulting mixture was stirred 4 h and was partitioned between EtOAc and water. The aqueous layer was acidified with aqueous HCl. The phases were separated, and the aqueous phase was extracted with EtOAc. The combined organic phase was dried over Na2SO4, filtered, and concentrated. The crude product was purified by silica gel chromatography (0-20% MeOH in DCM) to afford (R)-4-((R)-1-((5-(4-(4-acetylpiperazin-1-yl)phenyl)benzo[d]thiazol-7-yl)oxy)ethyl)pyrrolidin-2-one (4.31).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376441B2
Source datasetuspto-grants-2016_06
ORD IDord-347d790f2cad4db48fe0b03ca61685e5
Source noteuspto-grants-2016_06