HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2409925Generated: October 31, 2026
5-Bromo-2-(trifluoromethyl)pyrimidine → HCID 86690350, compound
https://huagongshe.com/reaction/2409925
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Bromo-2-(trifluoromethyl)pyrimidine | HCID 33697963 | — |
| Reactant | HCID 71233145 | HCID 71233145 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | HCID 86690350 | HCID 86690350 | 44.3% |
Reaction Steps
Dimethylacetamide (5.25 mL) was added to a round bottom flask containing tert-butyl (1R,2R)-2-(piperidin-3-ylamino)cyclohexylcarbamate (0.47 gm, 1.58 mmol) and 5-bromo-2-(trifluoromethyl)pyrimidine (0.43 gm, 1.89 mmol). The reaction mixture was then heated at 100° C. After 48 h heating was stopped. The reaction mixture was partitioned between EtOAc and sat. NaHCO3. The organic phase was isolated, washed with saturated aqueous NaCl, dried over MgSO4, filtered and concentrated. The resulting residue was purified using silica gel chromatography eluting with a gradient of 0-100% EtOAc/Hexanes holding at 100% EtOAc to give the diastereomeric product, tert-butyl (1R,2R)-2-(1-(2-(trifluoromethyl)pyrimidin-5-yl)piperidin-3-ylamino)cyclohexylcarbamate, (0.31 gm, 0.70 mmol, 44% yield) as light yellow solid. Anal. Calcd. for C21H32F3N5O2 m/z 443.3, found: 444.3 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08815909B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-6cd57cdc9f4c44a49bd0de4617de9c91 |
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| Source note | uspto-grants-2014_08 |
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