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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364699Generated: October 30, 2026

N-[[(2R)-4-benzylmorpholin-2-yl]methyl]-7-[[(7R)-8-cyclopentyl-7-ethyl-5-methyl-6-oxo-7H-pteridin-2-yl]amino]-2,3-dihydrobenzofuran-4-carboxamide → 7-[[(7R)-8-cyclopentyl-7-ethyl-5-methyl-6-oxo-7H-pteridin-2-yl]amino]-N-[[(2R)-4-methylmorpholin-2-yl]methyl]-2,3-dihydrobenzofuran-4-carboxamide

https://huagongshe.com/reaction/2364699

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[[(2R)-4-benzylmorpholin-2-yl]methyl]-7-[[(7R)-8-cyclopentyl-7-ethyl-5-methyl-6-oxo-7H-pteridin-2-yl]amino]-2,3-dihydrobenzofuran-4-carboxamideHCID 68108134—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product7-[[(7R)-8-cyclopentyl-7-ethyl-5-methyl-6-oxo-7H-pteridin-2-yl]amino]-N-[[(2R)-4-methylmorpholin-2-yl]methyl]-2,3-dihydrobenzofuran-4-carboxamideHCID 5103554918.5%

Reaction Steps

N-[[(2R)-4-Benzylmorpholin-2-yl]methyl]-7-[[(7R)-8-cyclopentyl-7-ethyl-5-methyl-6-oxo-7H-pteridin-2-yl]amino]-2,3-dihydrobenzofuran-4-carboxamide 15b (370 mg, 0.59 mmol) was dissolved in 30 mL of methanol. The reaction solution was hydrogenated with H-Cube (column of catalyst: 10% palladium/carbon; the pressure of hydrogen: 10 atmosphere; temperature: 40° C.) for 8 hours. The reaction solution was concentrated under reduced pressure to obtain the title compound 7-[[(7R)-8-cyclopentyl-7-ethyl-5-methyl-6-oxo-7H-pteridin-2-yl]amino]-N-[[(2R)-4-methylmorpholin-2-yl]methyl]-2,3-dihydrobenzofuran-4-carboxamide 15 (60 mg, yield: 18.5%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691822B2
Source datasetuspto-grants-2014_04
ORD IDord-18b01bbbc9f5451e946b1da59f8ef778
Source noteuspto-grants-2014_04