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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1352662Generated: November 3, 2026

1-Hydroxybenzotriazole → HCID 9804230, compound

https://huagongshe.com/reaction/1352662

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant4-Amino-1,2,2,6,6-pentamethylpiperidineHCID 693792—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant4-(5,6-dichloro-1H-benzimidazol-2-yl)benzoic acidHCID 4073119—
SolventTetrahydrofuranHCID 8028—
ProductHCID 9804230HCID 980423022%

Reaction Steps

A mixture of 5,6-dichloro-2-(4-carboxyphenyl)benzimidazole (0.3 g, 0.9 mmol) prepared as described in Preparation 8, 1-hydroxybenzotriazole (0.145 g, 1.08 mmol) and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (0.207 g, 1.08 mmol) in THF (10 ml) was heated at 35–40° C. for 1 h. 1,2,2,6,6,-Pentamethyl-4-aminopiperidine in THF (2 ml) was added dropwise and the reaction was refluxed for 1 h. After cooling to room temperature, the solvent was removed under reduced pressure and the residue was treated with 2N NaOH (5 ml). The solid was filtered, washed with water and dried at 50° C. under vacuum. The solid was suspended in isopropyl alcohol and stirred for half an hour, filtered and dried to give 91 mg of the title compound (yield 22%) as an yellow powder, mp>280° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07220769B2
Source datasetuspto-grants-2007_05
ORD IDord-175c97a8914a466f9e126cf341ba6d0f
Source noteuspto-grants-2007_05