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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2189831Generated: October 25, 2026

1-Butanol → HCID 178458666, compound

https://huagongshe.com/reaction/2189831

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ButanolHCID 263—
ReactantDiisopropylethylamineHCID 81531—
Reactant(R)-2-Amino-2-(4-fluorophenyl)ethanolHCID 10583003—
Reactant(S)-6-(5-Cyclopropyl-1H-pyrazol-3-ylamino)-5-fluoro-2-(1-(4-fluorophenyl)ethylamino)nicotinamideHCID 67455185—
ProductHCID 178458666HCID 17845866631%

Reaction Conditions

Temperature135 °C

Reaction Steps

2-Chloro-5-fluoro-6-(5-isopropoxy-1H-pyrazol-3-ylamino)nicotinonitrile (Method 2; 1.6 g, 5.0 mmol) and (R)-2-amino-2-(4-fluorophenyl)ethanol (2.0 g, 11.0 mmol) were added to a solution of n-BuOH (8 ml) and DIEA (0.8 g, 6.0 mmol) in a sealed tube. The reaction was heated to 135° C. for 72 hrs, cooled to 25° C., and concentrated. The resulting residue was purified by column chromatography (DCM-MeOH=50:1) to give the title compound (0.7 g, 31%). 1H NMR (400 MHz, CD3OD) δ 7.49 (d, J=9.5 Hz, 1H), 7.41-7.38 (m, 2H), 7.07-7.02 (m, 2H), 5.40 (s, 1H), 5.10-5.01 (m, 1H), 4.62-4.55 (m, 1H), 3.91-3.79 (m, 2H), 1.33-1.31 (m, 6H). MS: Calcd.: 414. Found: [M+H]+ 415.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08324252B2
Source datasetuspto-grants-2012_12
ORD IDord-11af05461baa455084bb8ed9627ff5b4
Source noteuspto-grants-2012_12