Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2183104Generated: October 30, 2026

HCID 22479987, compound → 3-(4-fluorophenyl)-1H-indazol-5-amine

https://huagongshe.com/reaction/2183104

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 22479987HCID 22479987—
CatalystHCID 178418390HCID 178418390—
SolventEthanolHCID 702—
Product3-(4-fluorophenyl)-1H-indazol-5-amineHCID 2248028453.1%

Reaction Steps

To a solution of 1-{[3-(4-fluorophenyl)-5-nitro(1H-indazolyl)]methoxy}-2-methoxyethane (100 mg, 0.29 mmol) in ethanol (30 mL) was added a scoup of Pd/carbon. The reaction was stirred overnight at room temperature under an atmosphere of hydrogen. It was filtered over celite and the solution concentrated to an oil. The oil was taken up in methanol (20 mL) and 6N HCl (20 mL) and the solution was heated to 75° C. for 3 hours. The solution was concentrated under vacuo, added to saturated bicarbonate (100 mL) and extracted with ethyl acetate (3×30 mL). The organic layers were dried (Na2SO4), concentrated to an oil and chromatographed on silica gel, eluting with 50% ethyl acetate/hexane to give the title compound (35 mg, 53% yield). 1H NMR (CDCl3) δ 10.1 (br s, 1H), 7.89 (dd, 1H), 7.23-7.16 (m, 4H), 6.91 (dd, 1H), 3.6 (br s, 1H); ES-MS (m/z) 228 [M+1 ]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06897231B2
Source datasetuspto-grants-2005_05
ORD IDord-2d6dc47acc894903990524de50015091
Source noteuspto-grants-2005_05