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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912112Generated: November 1, 2026

Trifluoroacetic acid → 5-(2-Morpholin-4-yl-7-pyridin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-pyrimidin-2-ylamine

https://huagongshe.com/reaction/912112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactantbis-(4-methoxy-benzyl)-[5-(2-morpholin-4-yl-7-pyridin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-pyrimidin-2-yl]-amineHCID 67386412—
CatalystSulfuric AcidHCID 1118—
Product5-(2-Morpholin-4-yl-7-pyridin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-pyrimidin-2-ylamineHCID 5924467026%

Reaction Conditions

Temperature40 °C

Reaction Steps

To the obtained bis-(4-methoxy-benzyl)-[5-(2-morpholin-4-yl-7-pyridin-4-yl-6,7-dihydro-5H-pyrrolo[2,3-d]pyrimidin-4-yl)-pyrimidin-2-yl]-amine, TFA (3 ml) and concentrated sulfuric acid (a few drops) were added, followed by stirring at 40° C. for 6 hours. This was concentrated under reduced pressure, and water was added, followed by neutralization with 1N aqueous sodium hydroxide solution. The resulting solid was purified by silica gel column chromatography (dichloromethane/2N ammonia methanol=40/1 to 10/1), to obtain the desired compound as a colorless solid (32.3 mg, yield 26%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08022205B2
Source datasetuspto-grants-2011_09
ORD IDord-951a58ac118541fe83cb28e8ef2e71c3
Source noteuspto-grants-2011_09