Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(4-Chlorophenoxy)-1-(piperazin-1-yl)ethanone | HCID 1074760 | — |
| Reactant | 4-Chloro-6-(4-fluorophenyl)thieno[2,3-d]pyrimidine | HCID 86662441 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 56941754 | HCID 56941754 | 75% |
Reaction Steps
To a solution of 4-chloro-6-(4-fluorophenyl)thieno[2,3-d]pyrimidine (20 mg, 0.08 mmol) and triethylamine (42 μl, 0.3 mmol) in dioxane (1 ml) was added 2-(4-chlorophenoxy)-1-(piperazin-1-yl)ethanone (25 mg, 0.1 mmol). The mixture was heated at 60° C. for 2 hours. After cooling down to room temperature, the solvents were removed under reduced pressure. The crude residue was purified by silica gel chromatography (CH2Cl2/MeOH 50:1) to yield the title compound as a white solid (27 mg, 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09193741B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-dae9b6eafa42477ba4c3f62dfe57cd45 |
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| Source note | uspto-grants-2015_11 |
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