HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1426408Generated: November 1, 2026
Sodium Iodide → 6-bromo-2-(pyrrolidin-1-ylmethyl)thieno[3,2-d]pyrimidin-4(3H)-one
https://huagongshe.com/reaction/1426408
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 6-bromo-2-(chloromethyl)thieno[3,2-d]pyrimidin-4(3H)-one | HCID 136333905 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-bromo-2-(pyrrolidin-1-ylmethyl)thieno[3,2-d]pyrimidin-4(3H)-one | HCID 136333906 | — |
Reaction Steps
To a mixture of pyrrolidine (2.2 mL), potassium carbonate (2.5 g), sodium iodide (134 mg) and N,N-dimethylformamide (40 mL) was added 6-bromo-2-(chloromethyl)thieno[3,2-d]pyrimidin-4(3H)-one (2.5 g), and the mixture was stirred at 70° C. for 30 min. Insoluble material was removed by filtration, the filtrate was concentrated under reduced pressure, and the residue was washed with a small amount of ethyl acetate to give the title compound (1.5 g) as a pale-yellow solid. The filtrate was purified by basic silica gel column chromatography (methanol/ethyl acetate) to give the title compound (0.87 g) as a pale-yellow solid. The total yield of the title compound was 2.37 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08933069B2 |
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| Source dataset | uspto-grants-2015_01 |
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| ORD ID | ord-a68f5727e6544b53aa79530e36fe1cf6 |
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| Source note | uspto-grants-2015_01 |
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