HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 4-Chlorothieno[2,3-d]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | thieno(2,3-d)pyrimidin-4(3H)-one | HCID 2808547 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Chlorothieno[2,3-d]pyrimidine | HCID 736618 | 97% |
Reaction Steps
To a solution of DMF (90 μL) and CH2Cl2 (2 mL) at 0° C. under N2, oxalyl chloride (148 mg, 1.2 mmol) is added slowly and stirred for 10 min. 3H-Thieno[2,3-d]pyrimid-4-one (81 mg, 0.52 mmol) is added as a solid to the solution and warmed with a heat gun until the solid dissolves. The reaction is stirred at 25° C. for 12 h under N2. The reaction mixture is poured into water and extracted with CH2Cl2 . The phases are separated and the organic layer is dried (Na2SO4) and stripped under reduced pressure to yield 4-chlorothieno[2,3-d]pyrimidine (87.6 mg, 97%) as a solid. 1H NMR (DMSO) δ 8.96 (1H, s), 8.17 (1H, d, J=6.0 Hz), 7.62 (1H, d, J=6.0 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06265410B1 |
| Source dataset | uspto-grants-2001_07 |
| ORD ID | ord-6a9e927e88004e5caa9e669e18db812f |
| Source note | uspto-grants-2001_07 |