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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695084Generated: November 1, 2026

Potassium Carbonate → N9-(3-Chloropropyl)-2-amino-6-chloropurine

https://huagongshe.com/reaction/1695084

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant6-ChloropurineHCID 5359277—
ReactantDMF 1-bromo-3-chloropropaneHCID 86615609—
SolventWaterHCID 962—
ProductN9-(3-Chloropropyl)-2-amino-6-chloropurineHCID 8582385036.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a stirred suspension of 6-chloropurine (5.0 g, 29.48 mmol) and K2CO3 (4.48 g, 32.42 mmol) in dry DMF 1-bromo-3-chloropropane (13.92 g, 88.45 mmol) is added. The reaction mixture is heated to 50° C. for 1 min and stirred at room temperature for additional 3 h. The reaction mixture is poured into 120 mL of water and extracted with CH2Cl2. The combined organic phases are washed with water, dried over MgSO4 and evaporated in vacuo. The residue is purified by flash column chromatography (dichloromethane/methanol 50:1 to 10:1) to yield 2.6 g (10.65 mmol, 35%) of the title compound as a colorless solid. 1H-NMR (400 MHz, DMSO-d6): δ=8.11 (s, 1H, H-8), 6.91 (s, 2H, NH2), 4.16 (t, J=6.8, 2H, CH2), 3.63 (t, J=6.8, 2H CH2), 2.25 (m, 2H, CH2) ppm. MS (ESI) m/z 247.3 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08163479B2
Source datasetuspto-grants-2012_04
ORD IDord-25928c8fa6354b1ca2f91a0da09e53cb
Source noteuspto-grants-2012_04