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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1882044Generated: November 2, 2026

1-Hydroxybenzotriazole → HCID 59331585, compound

https://huagongshe.com/reaction/1882044

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantAzetidine hydrochlorideHCID 12308726—
ReactantHCID 59331324HCID 59331324—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 59331585HCID 5933158553.3%

Reaction Steps

To a solution of [6-(5-{1-[4-(cyclopropylsulfonyl)phenyl]-2-(tetrahydro-2H-pyran-4-yl)ethyl}-1H-pyrrol-2-yl)pyridin-3-yl]acetic acid (0.200 g) in N,N-dimethylformamide (5 mL) were added azetidine hydrochloride (57 mg), triethylamine (0.169 mL), N-[3-(dimethylamino)propyl]-N′-ethylcarbodiimide hydrochloride (116 mg) and 1-hydroxybenzotriazole (93 mg), and the mixture was stirred at room temperature for 16 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The extract was washed successively with water and saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (ethyl acetate:methanol=100:0-80:20, volume ratio) and recrystallized from hexane-ethyl acetate to give the title compound (0.115 g, yield 53%) as colorless crystals. MS: 534 (MH+). melting point 94-98° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318746B2
Source datasetuspto-grants-2012_11
ORD IDord-18d1b948f8b347cdb3611a790bafe683
Source noteuspto-grants-2012_11