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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1449146Generated: October 27, 2026

Potassium Carbonate → 9-(2-Chloro-6-fluorobenzyl)-6-methylaminopurine

https://huagongshe.com/reaction/1449146

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantN6-MethyladenineHCID 67955—
Reactant1-Chloro-2-(chloromethyl)-3-fluorobenzeneHCID 108675—
SolventDimethylacetamideHCID 31374—
Product9-(2-Chloro-6-fluorobenzyl)-6-methylaminopurineHCID 12980163%

Reaction Steps

To a mixture of 7.45 g of 6-methylaminopurine, 6.9 g of potassium carbonate and 250 ml of N,N-dimethylacetamide was added 17.9 g of 2-chloro-6-fluorobenzyl chloride, and the resultant mixture was allowed to react at 110° C. for 6 hours with stirring. After cooling, the reaction mixture was filtered to remove insoluble materials and the filtrate was concentrated to dryness under reduced pressure. Upon addition of water to the resultant residue, the formed precipitate was collected by filtration and recrystallized from ethanol to give 9.08 g of 9-(2-chloro-6-fluorobenzyl)-6-methylaminopurine as colorless needles (yield: 63%), m.p. 188°-190° C. Nuclear magnetic resonance (NMR) spectrum of this product is identical with that of the corresponding compound synthesized in Example 1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04189485
Source datasetuspto-grants-1980_02
ORD IDord-c605836847a64024b165ecd66fba807a
Source noteuspto-grants-1980_02