HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1947656Generated: October 30, 2026
Cesium carbonate → Tert-butyl 1'-[2-(trifluoromethyl)pyrimidin-4-yl]-4,4'-bipiperidine-1-carboxylate
https://huagongshe.com/reaction/1947656
Participants
| Role | Name | HCID | Charge |
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| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 4,4'-Bipiperidine, 1-boc protected | HCID 11747599 | — |
| Reactant | 4-Bromo-2-(trifluoromethyl)pyrimidine | HCID 53302344 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | Tert-butyl 1'-[2-(trifluoromethyl)pyrimidin-4-yl]-4,4'-bipiperidine-1-carboxylate | HCID 59178917 | — |
Reaction Steps
The tert-butyl 4,4′-bipiperidine-1-carboxylate (28.5 mg, 0.11 mmol) and cesium carbonate (106 mg, 0.32 mmol) were stirred in NMP (0.5 ml) and the 4-bromo-2-(trifluoromethyl)pyrimidine (12 mg, 0.053 mmol) was added. The mixture was heated at 70° C. for 2 h. The reaction was cooled down to r.t. and diluted with ethyl acetate (5 mL) and was washed with water 2 mL (×1) and brine 2 mL (×1). The organic phase was dried over magnesium sulfate, filtered, and concentrated on rotavapor. The crude material was purified by preparative TLC with 30% acetone: hexane to yield the titled compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08399485B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-f44710e0fdbe4ca2997ba5e289987449 |
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| Source note | uspto-grants-2013_03 |
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