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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364749Generated: October 30, 2026

Sodium Carbonate → 7-[[(7R)-8-cyclopentyl-7-ethyl-5-methyl-6-oxo-7H-pteridin-2-yl]amino]-N-[(2S)-2-methoxy-3-(4-methylpiperazin-1-yl)propyl]-2,3-dihydrobenzofuran-4-carboxamide

https://huagongshe.com/reaction/2364749

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Reactant7-[[(7R)-8-cyclopentyl-7-ethyl-5-methyl-6-oxo-7H-pteridin-2-yl]amino]-2,3-dihydrobenzofuran-4-carboxylic acidHCID 68107475—
Reactant(2S)-2-methoxy-3-(4-methylpiperazin-1-yl)propan-1-amineHCID 68107783—
SolventDichloromethaneHCID 6344—
Product7-[[(7R)-8-cyclopentyl-7-ethyl-5-methyl-6-oxo-7H-pteridin-2-yl]amino]-N-[(2S)-2-methoxy-3-(4-methylpiperazin-1-yl)propyl]-2,3-dihydrobenzofuran-4-carboxamideHCID 5103658730%

Reaction Steps

7-[[(7R)-8-Cyclopentyl-7-ethyl-5-methyl-6-oxo-7H-pteridin-2-yl]amino]-2,3-dihydrobenzofuran-4-carboxylic acid 1q (100 mg, 0.23 mmol) and O-(benzotriazol-1-yl)-N,N,N′,N′-tetra methyluronium tetrafluoroborate (74 mg, 0.23 mmol) were dissolved in 20 mL of anhydrous dichloromethane followed by the addition of diisopropylethylamine (0.1 mL, 0.50 mmol) and the crude compound (2S)-2-methoxy-3-(4-methylpiperazin-1-yl)propan-1-amine 38b (43 mg, 0.23 mmol) successively. The reaction solution was stirred for 2 hours, added with 30 mL saturated sodium carbonate solution and extracted with dichloromethane (20 mL×3). The combined organic phase was washed with saturated sodium chloride solution (20 mL), then dried over anhydrous sodium 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-[(2S)-2-methoxy-3-(4-methylpiperazin-1-yl)propyl]-2,3-dihydrobenzofuran-4-carboxamide 38 (40 mg, yield: 30.0%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691822B2
Source datasetuspto-grants-2014_04
ORD IDord-e0fbbf0d24b542d8b65a229caf5ddf11
Source noteuspto-grants-2014_04