HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 4-Chlorothieno[3,2-d]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1,1-Dichloroethane | HCID 6365 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 3H,4H-thieno[3,2-d]pyrimidin-4-one | HCID 135417422 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Chlorothieno[3,2-d]pyrimidine | HCID 2735821 | 82% |
Reaction Steps
To a solution of DMF (170.3 μL, 2.2 mmol) and dichloroethane (1.2 mL) at 0° C. under N2, oxalyl chloride (279.2 mg, 3.2 mmol) is added slowly and stirred for 10 min. 3H-thieno[3,2-d]pyrimid-4-one (152.2 mg, 1.0 mmol) is added and refluxed for 5 h. The reaction mixture is poured into water and extracted with CH2Cl2. The organic layer is stripped under reduced pressure to yield 4-chlorothieno[3,2-d]pyrimidine (140 mg, 82%) as a yellow solid. 1H NMR (DMSO) δ 9.05 (1H, s), 8.62 (1H, d, J=5 Hz), 7.79 (1H, d, J=5 Hz)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06713484B2 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-4e2aeafd33734af78dfff5c9e8766ec8 |
| Source note | uspto-grants-2004_03 |