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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N6-Methyladenine | HCID 67955 | — |
| Reactant | 1-Chloro-2-(chloromethyl)-3-fluorobenzene | HCID 108675 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 9-(2-Chloro-6-fluorobenzyl)-6-methylaminopurine | HCID 129801 | 63% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04189485 |
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| Source dataset | uspto-grants-1980_02 |
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| ORD ID | ord-c605836847a64024b165ecd66fba807a |
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| Source note | uspto-grants-1980_02 |
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