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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

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Bromo-2-(trifluoromethyl)pyrimidineHCID 33697963—
ReactantHCID 71233145HCID 71233145—
SolventDimethylacetamideHCID 31374—
ProductHCID 86690350HCID 8669035044.3%

Reaction Conditions

Temperature100 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08815909B2
Source datasetuspto-grants-2014_08
ORD IDord-6cd57cdc9f4c44a49bd0de4617de9c91
Source noteuspto-grants-2014_08