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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2181626Generated: November 1, 2026

8-ethyl-7-(4-heptyl)-3-(4-methoxybenzyl)-1-methyl-3,7-dihydro-1H-purine-2,6-dione → HCID 11150504, compound

https://huagongshe.com/reaction/2181626

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-ethyl-7-(4-heptyl)-3-(4-methoxybenzyl)-1-methyl-3,7-dihydro-1H-purine-2,6-dioneHCID 69592598—
SolventTrifluoroacetic acidHCID 6422—
ProductHCID 11150504HCID 1115050497.3%

Reaction Steps

A solution of 8-ethyl-7-(4-heptyl)-3-[(4-methoxyphenyl)methyl]-1-methyl-3,7-dihydro-1H-purine-2,6-dione (4.30 g, 10.4 mmol) in trifluoroacetic acid (20 mL) was heated at 105° C. in a sealed tube for 14 h. The mixture was cooled to rt and concentrated. The residue was transferred to a separatory funnel containing saturated aqueous NaHCO3 (50 mL) and the aqueous layer was extracted with EtOAc (3×50 mL). The combined organic layers were washed with brine, dried over MgSO4, filtered, and concentrated. The residue was purified by column chromatography on silica gel (5% methanol in CH2Cl2) to afford 8-ethyl-7-(4-heptyl)-1-methyl-3,7-dihydro-1H-purine-2,6-dione (2.96 g, 97% yield) as a colorless solid: mp 152.5-153° C.; 1H NMR (300 MHz, CDCl3) δ 12.00 (s, 1H), 4.20-4.10 (m, 1H), 3.41 (s, 3H), 2.94 (q, J=7.3 Hz, 2H), 2.33-2.19 (m, 2H), 1.94-1.83 (m, 2H), 1.42 (t, J=7.4 Hz, 3H), 1.26-1.06 (m, 4H), 0.90 (t, J=7.3 Hz, 6H); LRMS (APCI) m/e 293.1 [(M+H)+, calcd for C15H25N4O2 293.2].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06894045B2
Source datasetuspto-grants-2005_05
ORD IDord-eaa7f06d25df48a3a8fddb6090151b28
Source noteuspto-grants-2005_05