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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339942Generated: October 30, 2026

Triethylamine → Methyl (4-{[[3-(6-amino-2-butoxy-8-oxo-7,8-dihydro-9H-purin-9-yl)propyl](3-piperidin-1-ylpropyl)amino]methyl}phenyl)acetate

https://huagongshe.com/reaction/339942

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantSodium CarbonateHCID 10340—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantMethyl 2-(4-formylphenyl)acetateHCID 19363032—
Reactant6-amino-2-butoxy-9-{3-[(3-piperidin-1-ylpropyl)amino]propyl}-7,9-dihydro-8H-purin-8-one dimaleateHCID 131732077—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductMethyl (4-{[[3-(6-amino-2-butoxy-8-oxo-7,8-dihydro-9H-purin-9-yl)propyl](3-piperidin-1-ylpropyl)amino]methyl}phenyl)acetateHCID 67989365—

Reaction Conditions

Temperature25 °C

Reaction Steps

A mixture of 6-amino-2-butoxy-9-{3-[(3-piperidin-1-ylpropyl)amino]propyl}-7,9-dihydro-8H-purin-8-one dimaleate (20.0 g, 31.3 mmol), triethylamine (9.5 g, 94.1 mmol) and NMP (72 g) was stirred at 25° C. for 30 min. Sodium triacetoxyborohydride (11.3 g, 53.3 mmol) was added to the solution and stirred for 15 min. A solution of methyl (4-formylphenyl)acetate (8.4 g, 47.1 mmol) in NMP (10.3 g g) was added to the solution and the mixture stirred for 8 hr. Then NMP (41 g) was poured into the reaction solution and cooled to 5° C. To the solution was added cold water (200 g) dropwise and the mixture stirred. The reaction mixture was adjusted to pH9 by using 10% aqueous Na2CO3 and water (86 g) added. After stirring for 1 hr, the reaction mixture was filtered, the collecting solid washed with cooled water and dried to give the crude subtitle compound as a white solid. Yield 15.0 g, 84%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895570B2
Source datasetuspto-grants-2014_11
ORD IDord-99505246748c4273a6f7c680e3f9d602
Source noteuspto-grants-2014_11