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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1689921Generated: October 30, 2026

Potassium Carbonate → HCID 57494063, compound

https://huagongshe.com/reaction/1689921

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 numberUS08153629B2
Source datasetuspto-grants-2012_04
ORD IDord-cab94f7059a24e508ed1c98bc09d574b
Source noteuspto-grants-2012_04