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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1189011Generated: November 1, 2026

1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → HCID 67118658, compound

https://huagongshe.com/reaction/1189011

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
ReactantEthylamine tetrahydrofuranHCID 66726184—
ReactantHCID 67118679HCID 67118679—
SolventDimethylformamideHCID 6228—
ProductHCID 67118658HCID 6711865870%

Reaction Steps

A mixture of [2-(7-methoxy-5-{[6-(methoxymethyl)pyridin-3-yl]oxy}-1H-indol-2-yl)-4,5-dihydro-1,3-thiazol-5-yl]acetic acid (300 mg), N-ethyl-N′-(3-dimethylaminopropyl)carbodiimide hydrochloride (268 mg), 1-hydroxybenzotriazole monohydrate (214 mg), 2M ethylamine tetrahydrofuran solution (0.7 mL) and N,N-dimethylformamide (10 mL) was stirred at room temperature for 16 h. The mixture was concentrated under reduced pressure. The residue was dissolved in water and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over magnesium sulfate, filtered and concentrated. The residue was purified by basic silica gel column chromatography (methanol/ethyl acetate/hexane=0/70/30 to 8/92/0, volume ratio) to give a pale yellow amorphous solid. The amorphous solid was crystallized from acetonitrile to give white crystals. The crystals were recrystallized from acetonitrile to give the title compound (222 mg, 70%) as colorless crystals. MS 455 (MH+). mp 130-132° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673942B2
Source datasetuspto-grants-2014_03
ORD IDord-86fd10e51379404aa55eaa86929dea44
Source noteuspto-grants-2014_03