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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 407465Generated: October 29, 2026

HCID 23139423, compound → HCID 23139425, compound

https://huagongshe.com/reaction/407465

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 23139423HCID 23139423—
SolventEthanolHCID 702—
ProductHCID 23139425HCID 2313942597%

Reaction Steps

SnCl22H2O (0.15 g, 0.66 mmol, 4.0 eq.) was added to a stirred solution of 5-(2-methoxy-5-nitro-phenyl)-1-methyl-3-trifluoromethyl-1H-pyrazole, see Example 1.99, (0.05 g, 0.16 mmol) in EtOH (2.0 mL). The mixture was stirred at reflux for 4 hrs and EtOH was removed under vacuum. The resulting solid was dissolved in EtOAc and 1N NaOH was added until the pH was adjusted to 6. The mixture was stirred overnight and filtered through celite. The aqueous phase was extracted with EtOAc (3×50 mL). The combined organic phase was dried over anhydrous MgSO4, filtered and evaporated to give 4-methoxy-3-(2-methyl-5-trifluoromethyl-2H-pyrazol-3-yl)-phenylamine (0.04 g, 0.15 mmol, 97% yield): LCMS m/z (%)=272 (M+H, 100). 1H NMR (400 MHz, CDCl3) δ: 6.82 (dd, J=16.0, 4.0 Hz, 1H), 6.79 (dd, J=10.0, 2.0 Hz, 1H), 6.61 (d, 1H), 6.46 (s, 1H), 3.76 (s, 3H), 3.74 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08754238B2
Source datasetuspto-grants-2014_06
ORD IDord-0e3deae0d4bf4eaaa27661cf41725bef
Source noteuspto-grants-2014_06