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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364753Generated: November 1, 2026

Sodium Carbonate → HCID 51036787, compound

https://huagongshe.com/reaction/2364753

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantDiisopropylethylamineHCID 81531—
ReactantO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
ReactantHCID 68107050HCID 68107050—
SolventDichloromethaneHCID 6344—
ProductHCID 51036787HCID 5103678769.2%

Reaction Steps

7-[[(7R)-8-Cyclopentyl-7-ethyl-5-methyl-6-oxo-7H-pteridin-2-yl]amino]-2-(methoxymethyl)-2,3-dihydrobenzofuran-4-carboxylic acid 40e (50 mg, 0.10 mmol) and O-(benzotriazol-1-yl)-N,N,N′,N′-tetra methyluronium tetrafluoroborate (33 mg, 0.10 mmol) were dissolved in 40 mL of dichloromethane followed by the addition of diisopropylethylamine (38 μL, 0.23 mmol) and 1-methyl-piperidyl-4-yl-amine (12 mg, 0.10 mmol) successively. The reaction solution was stirred for 1 hour, added with 20 mL of saturated sodium carbonate solution and extracted with dichloromethane (30 mL×3). The combined organic phase was washed with water (20 mL) and saturated sodium chloride solution (20 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]-2-(methoxymethyl)-N-(1-methyl-4-piperidyl)-2,3-dihydrobenzofuran-4-carboxamide 40 (40 mg, yield: 69.0%) as a light yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691822B2
Source datasetuspto-grants-2014_04
ORD IDord-dd70c0e9296a450b97ab6d4a84e061d3
Source noteuspto-grants-2014_04