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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 712247Generated: October 30, 2026

Water → Ethyl 4-(5-bromopyrimidin-2-ylamino)-1-methylcyclohexanecarboxylate

https://huagongshe.com/reaction/712247

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Bromo-2-chloropyrimidineHCID 606665—
ReactantEthyl 4-amino-1-methylcyclohexanecarboxylateHCID 58291914—
SolventEthanolHCID 702—
ProductEthyl 4-(5-bromopyrimidin-2-ylamino)-1-methylcyclohexanecarboxylateHCID 6697699419.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

To an ice-cold solution of ethyl 4-amino-1-methylcyclohexanecarboxylate (0.18 g, 0.97 mmol) in EtOH (5.0 mL) was added DIPEA (0.52 mL, 2.91 mmol) followed by the addition of 5-bromo-2-chloropyrimidine (0.185 g, 0.97 mmol). The mixture was heated to 80° C. for 6-8 h after then cooled to rt, water added and extracted with EtOAc (3×100 mL). The combined organics were washed with brine, dried over anhydrous Na2SO4, filtered and evaporated under reduced pressure. The crude residue was purified over 100-200 M silica-gel by using 4% EtOAc:hexane to obtain the desired product (0.064 g, 19%). MS: 342.01 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09181234B2
Source datasetuspto-grants-2015_11
ORD IDord-242d835b2ee14af2b83f77d8d840a3d5
Source noteuspto-grants-2015_11