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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2353164Generated: November 1, 2026

Potassium Carbonate → HCID 57494063, compound

https://huagongshe.com/reaction/2353164

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactanttert-butyl (3R,5S)-3,5-dimethylpiperazine-1-carboxylateHCID 10822535—
Reactant4-(6-(Bromomethyl)-2-chlorothieno[3,2-d]pyrimidin-4-yl)morpholineHCID 46180726—
SolventChloroformHCID 6212—
SolventAcetonitrileHCID 6342—
ProductHCID 57494063HCID 57494063—

Reaction Steps

A mixture of (3R,5S)-3,5-dimethyl-piperazine-1-carboxylic acid tert-butyl ester (0.92 g), 6-bromomethyl-2-chloro-4-morpholin-4-yl-thieno[3,2-d]pyrimidine (1 g) and potassium carbonate (1.59 g) in MeCN (10 ml) was heated to reflux for 5 days. The reaction mixture was subsequently cooled, diluted with chloroform, washed with brine and dried (MgSO4), and the solvent was removed in vacuo. The residue was purified by flash column chromatography to yield (3S,5R)-4-(2-chloro-4-morpholin-4-yl-thieno[3,2-d]pyrimidin-6-ylmethyl)-3,5-dimethyl-piperazine-1-carboxylic acid tert-butyl ester, 170 (1.2 g). Treatment of this compound with HCl in DCM/MeOH produced 2-chloro-6-(2S,6R)-2,6-dimethyl-piperazin-1-ylmethyl)-4-morpholin-4-yl-thieno[3,2-d]pyrimidine, 171, which was then methylated using 37% formaldehyde solution and sodium borohydride in MeOH, furnishing 172.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750002B2
Source datasetuspto-grants-2010_07
ORD IDord-cc2af554b7a54faba8db6557446dd10f
Source noteuspto-grants-2010_07