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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696796Generated: November 1, 2026

1-Hydroxybenzotriazole → HCID 66618584, compound

https://huagongshe.com/reaction/1696796

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 7H. 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 numberUS08163775B2
Source datasetuspto-grants-2012_04
ORD IDord-019b2b35f1e143859c8e4746c4d02e53
Source noteuspto-grants-2012_04