Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1481537Generated: October 31, 2026

3-Tert-butyl-isoxazole-5-carboxylic acid [2-methoxy-3-nitro-6-(2-trifluoromethyl-phenyl)-pyridin-4-yl]-amide → HCID 178494019, compound

https://huagongshe.com/reaction/1481537

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-Tert-butyl-isoxazole-5-carboxylic acid [2-methoxy-3-nitro-6-(2-trifluoromethyl-phenyl)-pyridin-4-yl]-amideHCID 67409916—
CatalystIronHCID 23925—
SolventAcetic AcidHCID 176—
ProductHCID 178494019HCID 178494019—

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 3-tert-butyl-isoxazole-5-carboxylic acid [2-methoxy-3-nitro-6-(2-trifluoromethyl-phenyl)-pyridin-4-yl]-amide (110 mg, 0.237 mmol, prepared as described in STEP C above) in AcOH (5 mL) was treated with iron powder (66.1 mg, 1.18 mmol), and the mixture was heated to 100° C. for 3 h. The AcOH was removed in vacuo. The residue was taken up in saturated aqueous NaHCO3 (50 mL) and extracted twice with EtOAc (50 mL). The combined organic extracts were dried over MgSO4 and concentrated in vacuo. The residue was purified on a 12-g SEPRA Si 50 SPE column (Flow rate=15 mL/min; Eluent=EtOAc-hexanes, 1:99 for 10 min, then 1:99 to 1:3 over 40 min). The chromatography was repeated as above to yield 2-(3-tert-butyl-isoxazol-5-yl)-4-methoxy-6-(2-trifluoromethyl-phenyl)-3H-imidazo[4,5-c]-pyridine as a white solid. Mass Spectrum (LCMS, APCI pos.): Calculated for C21H19N4O2F3: 417.1 (M+H). Measured: 417.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09409915B2
Source datasetuspto-grants-2016_08
ORD IDord-7184db4edc674a33869e3390a5f26de7
Source noteuspto-grants-2016_08