HuagongsheHuagongshe Chemistry Print Report · For research reference only
Bromine → 7-Bromothieno(3,2-d)pyrimidin-4-ol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Bromine | HCID 24408 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 3H,4H-thieno[3,2-d]pyrimidin-4-one | HCID 135417422 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | 7-Bromothieno(3,2-d)pyrimidin-4-ol | HCID 135743712 | 64% |
Reaction Steps
To a solution of 3H-thieno[3,2-d]pyrimid-4-one (82, 0.98 g, 6.4 mmol) in acetic acid (3.4 mL) was added a solution of bromine (1 mL) in acetic acid (3 mL). The reaction mixture was heated at reflux for 8 hours. The resulting suspension was allowed to cool to room temperature and then poured into a saturated aqueous solution of sodium bicarbonate to neutralize. The solid product was collected by vacuum filtration to give 7-bromo-3H-thieno[3,2-d]pyrimid-4-one (0.94 g, 64% yield) as a pale yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06503914B1 |
| Source dataset | uspto-grants-2003_01 |
| ORD ID | ord-1b9f44496fa444c79996d2a9e91ffdfb |
| Source note | uspto-grants-2003_01 |