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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2189877Generated: October 25, 2026

Diisopropylethylamine → (S)-6-(5-cyclopropyl-1H-pyrazol-3-ylamino)-5-fluoro-2-(1-(4-fluorophenyl)ethylamino)-4-iodonicotinonitrile

https://huagongshe.com/reaction/2189877

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant(S)-1-(4-Fluorophenyl)-ethylamineHCID 2779063—
Reactant2-chloro-6-(5-cyclopropyl-1H-pyrazol-3-ylamino)-5-fluoro-4-iodonicotinonitrileHCID 86620615—
Solvent1-ButanolHCID 263—
SolventWaterHCID 962—
Product(S)-6-(5-cyclopropyl-1H-pyrazol-3-ylamino)-5-fluoro-2-(1-(4-fluorophenyl)ethylamino)-4-iodonicotinonitrileHCID 6745677420%

Reaction Steps

A solution of 2-chloro-6-(5-cyclopropyl-1H-pyrazol-3-ylamino)-5-fluoro-4-iodonicotinonitrile (Method 39, 0.28 g, 0.69 mmol), (S)-1-(4-fluorophenyl)ethanamine (0.19 g, 1.3 mmol), and DIEA (0.11 g, 0.90 mmol) in n-BuOH (1 ml) was heated to 140° C. for 18 hours. The reaction was diluted with water (10 ml), extracted with DCM (2×20 ml) and the combined organic fractions were dried over Na2SO4, filtered, and then concentrated. The resulting oil was purified by column chromatography (DCM-MeOH=100:1) to give the title compound (0.07 g, 20%). MS: Calcd.: 506. Found: [M+H]+ 507.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324252B2
Source datasetuspto-grants-2012_12
ORD IDord-112a44ae7b954d78a203821d3f225711
Source noteuspto-grants-2012_12