HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 29886Generated: October 27, 2026
Chlorosuccinimide → 4,5-dichloro-7H-pyrrolo[2,3-d]pyrimidine
https://huagongshe.com/reaction/29886
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Chlorosuccinimide | HCID 31398 | — |
| Reactant | 4-Chloro-5-methyl-7H-pyrrolo(2,3-d)pyrimidine | HCID 14809282 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4,5-dichloro-7H-pyrrolo[2,3-d]pyrimidine | HCID 11106092 | 83% |
Reaction Steps
Following the procedure in Pdulo, J. S.; Saxena, N. K.; Nassiri, M. R.; Turk, S. R.; Drach, J. C.; Townsend, L. B. J. Med. Chem. 31:2086 (1988), 4-chloro-5-methyl-7H-pyrrolo[2,3-d]pyrimidine (Example 1A, 20. g, 0.13 mol) was suspended in anhydrous dichloromethane (500 mL), followed by addition of N-chlorosuccinimide (20.8 g, 0.160 mol). The reaction mixture was refluxed at 43° C. for 8 hours. The reaction was cooled down, and the white solid was filtered, washed with dichloromethane (300 mL), and dried to give 4,5-dichloro-7H-pyrrolo[2,3-d]pyrimidine (20 g, 83%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07423043B2 |
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| Source dataset | uspto-grants-2008_09 |
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| ORD ID | ord-924c8fe2692a4db982491774cdedb9b6 |
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| Source note | uspto-grants-2008_09 |
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