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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 882800Generated: October 31, 2026

Potassium Carbonate → (1R,3S,4S)-3-[(5-Bromo-pyrimidin-2-ylamino)-methyl]-2-aza-bicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl ester

https://huagongshe.com/reaction/882800

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-Bromo-2-chloropyrimidineHCID 606665—
Reactanttert-butyl (1R,3S,4S)-3-(aminomethyl)-2-azabicyclo[2.2.1]heptane-2-carboxylateHCID 66866957—
SolventO-XyleneHCID 7237—
Product(1R,3S,4S)-3-[(5-Bromo-pyrimidin-2-ylamino)-methyl]-2-aza-bicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl esterHCID 66867454—

Reaction Conditions

Temperature138 °C

Reaction Steps

5-Bromo-2-chloro-pyrimidine (8.62 mmol) is added to a solution of (1R,3S,4S)-3-aminomethyl-2-aza-bicyclo[2.2.1]heptane-2-carboxylic acid tert-butyl ester (6.63 mmol) in o-xylene (25 mL). K2CO3 (20.0 mmol) and DIPEA (19.9 mmol) are added successively and the mixture is heated to 138° C. for 16 h. The mixture is cooled to rt and filtered. The residue is washed with DCM and the combined filtrates are concentrated in vacuo to give the desired product which is used without further purification. LC-MS: tR=1.09 min; [M+H]+=383.3.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08236801B2
Source datasetuspto-grants-2012_08
ORD IDord-a91eae23f64341bb91499d271d16dbf5
Source noteuspto-grants-2012_08