HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114606Generated: October 31, 2026
Bromocyclopentane → 4-Chloro-7-cyclopentyl-7H-pyrrolo[2,3-d]pyrimidine
https://huagongshe.com/reaction/2114606
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromocyclopentane | HCID 8728 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 7H-Pyrrolo(2,3-d)pyrimidine, 4-chloro- | HCID 5356682 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Chloro-7-cyclopentyl-7H-pyrrolo[2,3-d]pyrimidine | HCID 519848 | 75.3% |
Reaction Steps
NaH (3.8 g, 95.3 mmol) was added to a solution of 4-Chloro-7H-pyrrolo[2,3-d]pyrimidine (10 g, 63.5 mmol) in DMF (50 mL) at 0° C. The resulting mixture was stirred at 0° C. for 30 min, then warmed to room temperature. At this time Cyclopentylbromide (18.9 g, 127 mmol) was added and the reaction was heated to 60° C. After 4 h the reaction was cooled to 0° C. and quenched slowly with water. The aqueous layer was extracted with EtOAc (3×), the combined organic layers were washed with water (1×), dried over Na2SO4, and concentrated. Purification by flash column chromatography (Hexanes/Ethyl acetate 9:1) afforded the title compound (10.6 g, 75%). MS: 222.1/224.1 (MH+); retention time 5.77 min. (HPLC method 4).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07435739B2 |
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| Source dataset | uspto-grants-2008_10 |
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| ORD ID | ord-71395d6fa9634015a4df40f75c5b6e21 |
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| Source note | uspto-grants-2008_10 |
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