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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2247773Generated: October 26, 2026

1-Hydroxybenzotriazole → (5-(5-(4-Isobutyl-3-methylphenyl)-1,2,4-oxadiazol-3-yl)pyridin-2-yl)methanol

https://huagongshe.com/reaction/2247773

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant4-Isobutyl-3-methylbenzoic acidHCID 59272938—
Reactant6-({[t-Butyl(dimethyl)silyl]oxy}methyl)-N'-hydroxypyridine-3-carboximidamideHCID 86620225—
SolventTetrahydrofuranHCID 8028—
Product(5-(5-(4-Isobutyl-3-methylphenyl)-1,2,4-oxadiazol-3-yl)pyridin-2-yl)methanolHCID 68523492—

Reaction Steps

The crude product of the title compound was synthesized by conducting the similar reaction to that mentioned in Example 12 (12a) using 4-isobutyl-3-methylbenzoic acid (0.12 g, 0.61 mmol) that was obtained in Example 27 (27d), 1-hydroxybenzotriazole (86 mg, 0.64 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.12 g, 0.64 mmol), 6-({[t-butyl(dimethyl)silyl]oxy}methyl)-N′-hydroxypyridine-3-carboximidamide (0.16 g, 0.58 mmol) that was obtained in Example 23 (23c), and tetrabutylammonium fluoride (a 1.0 M solution in tetrahydrofuran, 1.2 ml, 1.2 mmol). Subsequently, the crude product of the title compound thus obtained was purified by chromatography on a silica gel column using a mixed solvent of ethyl acetate and hexane (2:3 to 1:1) as the eluent to afford the title compound (0.19 g) in a yield of 99% as a white crystalline solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687491B2
Source datasetuspto-grants-2010_03
ORD IDord-8719682d7c624eb890000ae6645667a8
Source noteuspto-grants-2010_03