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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364710Generated: November 1, 2026

Diisopropylethylamine → 7-[[(7R)-8-cyclopentyl-7-ethyl-5-methyl-6-oxo-7H-pteridin-2-yl]amino]-N-[(2R)-3-(4-methylpiperazin-1-yl)-2-hydroxy-propyl]-2,2-dimethyl-3H-benzofuran-4-carboxamide

https://huagongshe.com/reaction/2364710

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantSodium BicarbonateHCID 516892—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant(2R)-1-amino-3-(4-methylpiperazin-1-yl)propan-2-olHCID 28279114—
Reactant7-[[(7R)-8-cyclopentyl-7-ethyl-5-methyl-6-oxo-7H-pteridin-2-yl]amino]-2,2-dimethyl-3H-benzofuran-4-carboxylic acidHCID 68107473—
SolventDichloromethaneHCID 6344—
Product7-[[(7R)-8-cyclopentyl-7-ethyl-5-methyl-6-oxo-7H-pteridin-2-yl]amino]-N-[(2R)-3-(4-methylpiperazin-1-yl)-2-hydroxy-propyl]-2,2-dimethyl-3H-benzofuran-4-carboxamideHCID 5103576377.4%

Reaction Steps

7-[[(7R)-8-Cyclopentyl-7-ethyl-5-methyl-6-oxo-7H-pteridin-2-yl]amino]-2,2-dimethyl-3H-benzofuran-4-carboxylic acid 4f (116 mg, 0.25 mmol) was dissolved in 15 mL of dichloromethane followed by the addition of (2R)-1-amino-3-(4-methylpiperazin-1-yl)propan-2-ol 20e (48 mg, 0.28 mmol), O-(benzotriazol-1-yl)-N,N,N′,N′-tetra methyluronium tetrafluoroborate (80 mg, 0.25 mmol) and diisopropylethylamine (97 mg, 0.75 mmol). The reaction solution was stirred for 2 hours. The resulting solution was added with 20 mL of saturated sodium bicarbonate solution and extracted with dichloromethane (50 mL×3). The combined organic phase was washed with water (50 mL), saturated sodium chloride solution (50 mL) successively, then dried over anhydrous magnesium sulfate, filtered and the filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain the title compound 7-[[(7R)-8-cyclopentyl-7-ethyl-5-methyl-6-oxo-7H-pteridin-2-yl]amino]-N-[(2R)-3-(4-methylpiperazin-1-yl)-2-hydroxy-propyl]-2,2-dimethyl-3H-benzofuran-4-carboxamide 20 (120 mg, yield: 77.4%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691822B2
Source datasetuspto-grants-2014_04
ORD IDord-400c803f2b7a428eb2c3bfdb1f155832
Source noteuspto-grants-2014_04