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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1527276Generated: November 5, 2026

Trifluoroacetic acid → 2-(3-(2-Hydroxyacetyl)-1H-indazol-1-yl)acetic acid

https://huagongshe.com/reaction/1527276

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantBistrifluoroacetoxyiodobenzeneHCID 12041285—
Reactant2-(3-Acetyl-1H-indazol-1-yl)acetic acidHCID 68284715—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
Product2-(3-(2-Hydroxyacetyl)-1H-indazol-1-yl)acetic acidHCID 68283722—

Reaction Conditions

Temperature90 °C

Reaction Steps

The title compound was prepared in a similar manner as described by N. Yoshikawa et al., J. Org. Chem., 2002, 67, 2556-2565: A mixture of 2-(3-acetyl-1H-indazol-1-yl)acetic acid (100 mg, 0.46 mmol), TFA (0.71 mL, 0.92 mmol) and bis-(trifluoroacetoxy)-iodobenzene (394 mg, 0.92 mmol) in CH3CN (4 mL) and water (0.6 mL) was heated to reflux (90° C.) for 16 h. Solvents were evaporated and the crude product was purified by preparative HPLC (Waters Sunfire, C18-ODB, 5 μm, 30×100 mm, flow: 40 mL/min, eluent: 5-100% CH3CN/H2O/20 min, 100% CH3CN/2 min, CH3CN and H2O containing 0.1% TFA) to give after lyophilization of the purified fractions the title compound. MS (LC-MS): 233 [M+H]+; tR (HPLC conditions k): 2.41 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085555B2
Source datasetuspto-grants-2015_07
ORD IDord-ea5632ca86c94bb49fc12aa51cc33a4d
Source noteuspto-grants-2015_07