HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 718234Generated: October 30, 2026
Triethylamine → 2-(4-Chlorophenoxy)-1-(4-(2-(4-fluorophenyl)-5-methylthiazolo[5,4-d]pyrimidin-7-yl)piperazin-1-yl)ethanone
https://huagongshe.com/reaction/718234
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(4-Chlorophenoxy)-1-(piperazin-1-yl)ethanone | HCID 1074760 | — |
| Reactant | 7-Chloro-2-(4-fluorophenyl)-5-methylthiazolo[5,4-d]pyrimidine | HCID 86662439 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-(4-Chlorophenoxy)-1-(4-(2-(4-fluorophenyl)-5-methylthiazolo[5,4-d]pyrimidin-7-yl)piperazin-1-yl)ethanone | HCID 46916478 | 75% |
Reaction Steps
To a solution of 7-chloro-2-(4-fluorophenyl)-5-methylthiazolo[5,4-d]pyrimidine (30 mg, 0.11 mmol) and triethylamine (22 μl, 0.16 mmol) in dioxane (1 ml) was added 2-(4-chlorophenoxy)-1-(piperazin-1-yl)ethanone (38 mg, 0.16 mmol). The reaction mixture was heated at 70° C. for 3 hours. After cooling, the volatiles were removed under reduced pressure. The crude residue was purified by chromatography on silica gel (CH2Cl2/MeOH 70:1) to yield the title compound as a white solid (40 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-dcddfdca619d46f38aa6bfcbbcc1fc4e |
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| Source note | uspto-grants-2015_11 |
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