HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728801Generated: October 29, 2026
Potassium Carbonate → HCID 14306333, compound
https://huagongshe.com/reaction/728801
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 3-(Bromomethyl)thiophene | HCID 520703 | — |
| Reactant | 2-Amino-6-chloropurine | HCID 5360349 | — |
| Reactant | Dichloromethane methanol | HCID 21226129 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 14306333 | HCID 14306333 | — |
Reaction Steps
A mixture of 2-amino-6-chloropurine (Aldrich Chemical Co.) (7.47 g; 0.44 mol), potassium carbonate (6.64 g; 0.048 mol), and 3-thenylbromide (see U.S. Pat. No. 3,746,724) (7.8 g; 0.044 mol) in DMF (200 ml) was stirred under nitrogen at room temperature for 48 hours. The mixture was filtered and the filtrate evaporated to dryness under vacuum, ethyl ether was addedand the precipitate was collected by filtration to give a mixture of 7- and9-substituted chloropurines. A sample of pure 9isomer was prepared by chromatography on silica gel with 5% methanol/methylene chloride as the eluting solvent to separate it from the 7-isomer. Analytical sample was obtained by crystallization from acetonemethanol mixture, yield 2.36 g, mpsoftens at 185° C. (dec) and then melts at 203°-204° C. (dec).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05051429 |
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| Source dataset | uspto-grants-1991_09 |
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| ORD ID | ord-b1b9522c44fc467198a6d779c091e039 |
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| Source note | uspto-grants-1991_09 |
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