HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1487243Generated: October 30, 2026
N-Iodosuccinimide → 2-Butyl-4-chloro-7-iodo-5H-pyrrolo[3,2-d]pyrimidine
https://huagongshe.com/reaction/1487243
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Iodosuccinimide | HCID 120273 | — |
| Reactant | 2-Butyl-4-chloro-5H-pyrrolo[3,2-d]pyrimidine | HCID 118382848 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | tert-Butyl methyl ether | HCID 15413 | — |
| Product | 2-Butyl-4-chloro-7-iodo-5H-pyrrolo[3,2-d]pyrimidine | HCID 118382847 | 81.3% |
Reaction Steps
N-Iodosuccinimide (2.09 g, 9.29 mmol) was added portionwise to a stirred solution of 2-butyl-4-chloro-5H-pyrrolo[3,2-d]pyrimidine (1.69 g, 8.06 mmol) in THF (35 mL). The resultant mixture was stirred at room temperature for 1 hour. The reaction mixture was diluted with TBME (50 mL) then washed with aqueous sodium thiosulphate solution (50 mL) then saturated aqueous sodium chloride solution (20 mL). The organic phase was dried (Na2SO4), filtered and evaporated. The sample was dissolved in dichloromethane and purified by chromatography on silica using a gradient of 0-100% dichloromethane-cyclohexane over 30 minutes followed by a gradient of 0-100% TBME-cyclohexane followed by 0-20% methanol over 15 minutes. The appropriate fractions were identified by LC-MS then combined and evaporated in vacuo to give the title compound as a yellow solid (2.2 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09428512B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-42c0e598aeba4a2cae89c79fd0efaa12 |
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| Source note | uspto-grants-2016_08 |
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