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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172735Generated: November 2, 2026

1-Hydroxybenzotriazole → HCID 66618584, compound

https://huagongshe.com/reaction/1172735

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-((Tert-butoxy)carbonyl)piperidine-3-carboxylic acidHCID 2735647—
ReactantHCID 178491258HCID 178491258—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 66618584HCID 6661858472%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of N-Hydroxy-4-methoxy-benzamidine (0.20 g, 1.50 mmol), 1-Boc-piperidine-3-carboxylic acid (0.34 g, 1.50 mmol), HOBT (0.23 g, 1.50 mmol) and EDCI.HCl (0.43 g, 2.25 mmol) in dioxane (2.5 ml) was stirred at R.T for 7 H. After this time the mixture was heated at 80° C. overnight with the carousel Radley's. The mixture was concentrated. The organic layer was washed with water, NaOH 1N and water. The organic layer was dried over Na2SO4, filtered and evaporated. The crude product was purified by flash chromatography (DCM/MeOH: 99/1) to afford 0.39 mg (72%) of 3-[3-(4-Methoxy-phenyl)-[1,2,4]oxadiazol-5-yl]-piperidine-1-carboxylic acid tert-butyl ester as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834035B2
Source datasetuspto-grants-2010_11
ORD IDord-ecd5040f400c4d5db8f6b9cb3b6f4cee
Source noteuspto-grants-2010_11