Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Bromine | HCID 24408 | — |
| Edukt | Thieno(3,2-d)pyrimidine-2,4(1H,3H)-dione | HCID 7059273 | — |
| Lösungsmittel | Acetic Acid | HCID 176 | — |
| Produkt | 7-Bromothieno[3,2-d]pyrimidine-2,4(1h,3h)-dione | HCID 18326427 | 60% |
Reaktionsschritte
Thieno[3,2-d]pyrimidine-2,4(1H,3H)-dione (10.38 g, 61.72 mmol) was dissolved in acetic acid (230 mL) and Bromine (11.13 mL, 216 mmol) was added. The reaction was heated at 80° C. for 3.5 h. Complete reaction was confirmed by LCMS. The reaction mixture was poured onto ice water slowly and filtered off the precipitate which was dried overnight under vacuum to give 7-bromothieno[3,2-d]pyrimidine-2,4(1H,3H)-dione (9.1 g, 60% yield)
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08883799B2 |
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| Quelldatensatz | uspto-grants-2014_11 |
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| ORD ID | ord-2b62709c92634f6d93054bc037e3db69 |
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| Quellennotiz | uspto-grants-2014_11 |
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