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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1167555Generated: October 29, 2026

2-Fluoroaniline → HCID 178505594, compound

https://huagongshe.com/reaction/1167555

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FluoroanilineHCID 9584—
ReactantHCID 178505591HCID 178505591—
CatalystMethanolHCID 887—
ProductHCID 178505594HCID 17850559477%

Reaction Conditions

Temperature180 °C

Reaction Steps

A mixture of 2-chloro-4-[3-(4-fluorophenyl)-1H-pyrazol-4-yl]pyrimidine (0.37 g; 0.0013 mol; prepared as set forth in Example A-299), 7 mL of 2-fluoroaniline and 2 drops of methanol was heated at 180° C. in a sealed tube for 16 hours. Excess amine was removed by vacuum distillation and the residue was treated with ethyl acetate to give 0.35 g of N-(2-fluorophenyl)-4-[3-(4-fluorophenyl)-1H-pyrazol-4-yl]-2-pyrimidinamine as a yellow solid (77%), mp: 239-240° C. Anal. Calc'd. for C19H13F2N5: C, 65.33; H, 3.75; N, 20.05. Found: C, 64.95; H, 3.80; N, 19.77.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06617324B1
Source datasetuspto-grants-2003_09
ORD IDord-7e475f50145b45d1976dbfd50559671e
Source noteuspto-grants-2003_09