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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1432378Generated: November 3, 2026

Dichloromethane → 1-[9-Cyclopentyl-6-(3,4-dimethoxy-benzylamino)-9H-purin-2-yl]-piperidin-3-ol

https://huagongshe.com/reaction/1432378

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantPotassium CarbonateHCID 11430—
ReactantPiperidine-3-ol hydrochlorideHCID 2723962—
Reactant(2-Chloro-9-cyclopentyl-9H-purin-6-yl)-(3,4-dimethoxy-benzyl)-amineHCID 18002120—
Solvent2,5-DimethylpyridineHCID 11526—
Product1-[9-Cyclopentyl-6-(3,4-dimethoxy-benzylamino)-9H-purin-2-yl]-piperidin-3-olHCID 1018254082%

Reaction Conditions

Temperature180 °C

Reaction Steps

(2-Chloro-9-cyclopentyl-9H-purin-6-yl)-(3,4-dimethoxy-benzyl)-amine (446 mg, 1.15 mmol), 3-hydroxypiperidine hydrochloride (791 mg, 5.75 mmol) and K2CO3 (1.19 mg, 8.63 mmol) were suspended in 2,5-lutidine (10 mL) and the mixture was heated at 180° C. for 4 h. After cooling, CH2Cl2 (50 mL) was added and the solution was extracted with brine (2×15 mL). The organic fraction was dried over MgSO4, filtered and evaporated. The residue was purified by flash chromatography (95:5 CH2Cl2/MeOH) to afford the title compound as an off-white foam (427 mg, %). Anal. RP-HPLC (Phenomenex Jupiter, 5 μ, C18, 300 Å, 4.6×250 mm; 1 mL/min): tR=18.4 min (10-70% MeCN in 0.1% aq CF3COOH over 20 min); tR=16.0 min (35-45% MeCN in 0.1% aq CF3COOH over 20 min); purity>95% (λ=214 nm). DE-MALDI-TOF MS: [M+H]+=453.9 (C24H32N6O3=452.6).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07612079B2
Source datasetuspto-grants-2009_11
ORD IDord-903656498db8447eba1bf7e71be6e6fd
Source noteuspto-grants-2009_11