HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 7-bromo-4-chloro-5H-pyrrolo[3,2-d]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | 4-chloro-5H-pyrrolo[3,2-d]pyrimidine | HCID 5370695 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 7-bromo-4-chloro-5H-pyrrolo[3,2-d]pyrimidine | HCID 52987660 | — |
Reaction Steps
To 4-chloro-5H-pyrrolo[3,2-d]pyrimidine (100 mg), tetrahydrofuran (5 mL) was added, and N-bromosuccinimide (116 mg) was further added thereto, followed by stirring for 1 hour. After completion of the reaction, the reaction mixture was mixed with ethyl acetate and washed with water. The washed mixture was dried over anhydrous sodium sulfate, and filtered and distilled under reduced pressure to obtain the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08853213B2 |
| Source dataset | uspto-grants-2014_10 |
| ORD ID | ord-cf21458fd1b4488ebd2201ecfae11a77 |
| Source note | uspto-grants-2014_10 |