Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465182Generated: November 1, 2026

1-propyl-1H-pyrazole-3-carboxylic acid → HCID 56847363, compound

https://huagongshe.com/reaction/1465182

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-propyl-1H-pyrazole-3-carboxylic acidHCID 6485387—
Reactant4-((6,7-Dimethoxyquinolin-4-yl)oxy)-3-fluorobenzenamineHCID 11426997—
ProductHCID 56847363HCID 5684736317%

Reaction Steps

C1 was prepared from A2 and 1-propylpyrazole-3-carboxylic acid following the general procedure reported in Preparative Example 11. The residue was purified by reverse phase RP-HPLC (column: C18), using H2O and ACN as eluents. The desired fractions were lyophilized to yield the title compound C1 (46 mg, 0.10 mmol, 17%) as a white powder. 1H NMR (400 MHz, d6-DMSO, 300K) δ 0.85 (t, J=7.3 Hz, 3H), 1.86 (sext., J=7.3 Hz, 2H), 3.94 (s, 6H), 4.18 (t, J=7.3 Hz, 2H), 6.45 (d, J=5.1 Hz, 1H), 6.79 (d, J=2.3 Hz, 1H), 7.39 (s, 1H), 7.42 (t, J=9.0 Hz, 1H), 7.52 (s, 1H), 7.78 (d, J=9.0 Hz, 1H), 7.90 (d, J=2.3 Hz, 1H), 8.05 (dd, J=13.4 Hz, J=2.3 Hz, 1H), 8.46 (d, J=5.2 Hz, 1H), 10.34 (s, 1H). MS (ES) C24H23FN4O4 requires: 450. Found: 451 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999982B2
Source datasetuspto-grants-2015_04
ORD IDord-567023d01889469da051506100abee25
Source noteuspto-grants-2015_04