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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2256372Generated: October 29, 2026

4-Fluorophenyl isocyanate → HCID 18969254, compound

https://huagongshe.com/reaction/2256372

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorophenyl isocyanateHCID 70955—
ReactantN-[2-(4-amino-1-piperidinyl)ethyl]-1-(2-propyl)-1H-indazole-3-carboxamide dioxalateHCID 86751129—
SolventTetrahydrofuranHCID 8028—
ProductHCID 18969254HCID 18969254—

Reaction Conditions

Temperature10 °C

Reaction Steps

The product from Example 23, as the free base (0.330 g, 1 mmol) was stirred in 8 mL tetrahydrofuran and cooled in an ice bath to 10° C. To the mixture was added dropwise 4-fluorophenyl isocyanate (0.11 mL, 1 mmol) and the resulting mixture was stirred 1.5 h at room temperature and filtered, and the filtrate was evaporated to an oil. Crystallization as the oxalate salt from ethyl acetate/methanol provided 0.147 g colorless crystals. Mp 158° C. Mass spectrum, m+ =466. Anal (C27H33FN6O6) theory C, 58.27; H, 5.98; N, 15.10; found C, 58.48; H, 6.23; N, 14.94.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05654320
Source datasetuspto-grants-1997_08
ORD IDord-e680c14dd85a43b0b2f3c5f0f9048e3e
Source noteuspto-grants-1997_08