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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 510853Generated: October 31, 2026

Diisopropylethylamine → N-{1-[4-chloro-3'-fluoro-5-methyl-6-(4H-1,2,4-triazol-4-yl)biphenyl-2-yl]ethyl}-9H-purin-6-amine

https://huagongshe.com/reaction/510853

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-[4-Chloro-3'-fluoro-5-methyl-6-(4H-1,2,4-triazol-4-yl)biphenyl-2-yl]ethanamineHCID 86666781—
ReactantHCID 178419477HCID 178419477—
SolventIsopropanolHCID 3776—
ProductN-{1-[4-chloro-3'-fluoro-5-methyl-6-(4H-1,2,4-triazol-4-yl)biphenyl-2-yl]ethyl}-9H-purin-6-amineHCID 178427927—

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 6-bromo-9H-purine (10 mg, 0.050 mmol), 1-[4-chloro-3′-fluoro-5-methyl-6-(4H-1,2,4-triazol-4-yl)biphenyl-2-yl]ethanamine (15 mg, 0.045 mmol), and N,N-diisopropylethylamine (0.016 mL, 0.091 mmol) in isopropyl alcohol (0.2 mL) was heated at 90° C. under nitrogen overnight. The mixture was evaporated and the resulting mixture was purified on RP-HPLC (XBridge C18 Column, eluting with a gradient of acetonitrile in water with 0.2% ammonium hydroxide, at flow rate of 30 mL/min) to give the desired product. LCMS calculated for C22H19ClFN8 (M+H)+: m/z=449.1. found: 449.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09096600B2
Source datasetuspto-grants-2015_08
ORD IDord-4e3f93ac4e094dc3bc04819eaa32f539
Source noteuspto-grants-2015_08