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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1693572Generated: October 31, 2026

HCID 67282126, compound → HCID 57897836, compound

https://huagongshe.com/reaction/1693572

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67282126HCID 67282126—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 57897836HCID 57897836—
ProductHCID 86634698HCID 86634698—

Reaction Steps

A solution of N-[2-biphenyl-4-yl-1-(4-chloro-phenyl)-6-oxo-9-phenyl-6,9-dihydro-1H-purin-8-ylmethyl]-N-(4-methoxy-benzyl)-methanesulfonamide (18 mg, 0.026 mmol) in TFA (1 mL) was heated at 90° C. in a sealed tube for 12 h. The reaction mixture was concentrated in vacuo and the resulting crude oil was purified by flash chromatography (silica, 5% MeOH/CH2Cl2) to give the title compound Ar-[2-biphenyl-4-yl-1-(4-chloro-phenyl)-6-oxo-9-phenyl-6,9-dihydro-1H-purin-8-ylmethyl]-methanesulfonamide as a white solid. 1H NMR (CDCl3) δ (ppm) 7.64 7.54 (m, 3H), 7.51 7.45 (m, 4H), 7.44 7.38 (m, 4H), 7.37 7.30 (m, 4H), 7.28 (s, 1H), 7.13 (d, 2H), 5.92 (br s, 1H), 4.48 (s, 2H), 2.99 (s, 3H); HPLC-MS calculated for C31H24ClN5O3S (M+H+): 582.1. Found 582.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158634B2
Source datasetuspto-grants-2012_04
ORD IDord-2a21d47aa49249a29d0d163407c44741
Source noteuspto-grants-2012_04