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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912138Generated: October 31, 2026

4-chloro-2-morpholin-4-yl-7-pyridin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidine → HCID 67385657, compound

https://huagongshe.com/reaction/912138

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-chloro-2-morpholin-4-yl-7-pyridin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidineHCID 59244708—
ReactantHCID 86640120HCID 86640120—
ReactantButyllithiumHCID 178418339—
ReactantHCID 178418918HCID 178418918—
CatalystZincchlorideHCID 3007855—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67385657HCID 673856577.1%

Reaction Steps

To a solution of n-butyl lithium (1.56M hexane solution, 0.23 ml, 0.363 mmol) in tetrahydrofuran (2 ml), at 0° C., isopropyl magnesium chloride (2M tetrahydrofuran solution, 0.09 ml, 0.182 mmol) was added, followed by stirring for 15 minutes. To this, a solution of (6-bromo-pyridin-3-yl)-bis-(4-methoxy-benzyl)-amine (50 mg, 0.121 mmol, 1.0 equivalent) in tetrahydrofuran (1 ml) was added, followed by stirring for 1.5 hours. Zinc chloride (1M diethyl ether solution, 0.55 ml, 0.545 mmol) was added, and the temperature was raised to room temperature, followed by stirring for 1 hour. 4-Chloro-2-morpholin-4-yl-7-pyridin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidine (38.4 mg, 0.121 mmol) was added, followed by refluxing for 2 hours. Water was added, followed by extraction with ethyl acetate, and the organic layer was washed with brine. After drying over sodium sulfate, concentration was carried out under reduced pressure. Purification by preparative TLC (dichloromethane/methanol=40/1) afforded bis-(4-methoxy-benzyl)-[6-(2-morpholin-4-yl-7-pyridin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-pyridin-3-yl]-amine (5.3 mg, yield 7%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022205B2
Source datasetuspto-grants-2011_09
ORD IDord-be4341fbab6e4b5f843137cc16ad4ed3
Source noteuspto-grants-2011_09