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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889287Generated: October 31, 2026

1-Hydroxybenzotriazole → HCID 68841966, compound

https://huagongshe.com/reaction/1889287

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl 2-aminoisobutyrate hydrochlorideHCID 13258034—
ReactantHCID 68840681HCID 68840681—
SolventDimethylformamideHCID 6228—
ProductHCID 68841966HCID 68841966—

Reaction Conditions

Temperature0 °C

Reaction Steps

At 0° C. to a solution of 165 mg of a mixture of the (E)- and (Z)-isomers of 1-(4-phenyl-but-1-enyl)-naphthalene-2-carboxylic acid in 2 ml abs. DMF under inert atmosphere 95 mg 1-hydroxybenzotriazole, 110 μl N,N′-diiospropylcarbodiimide and 98 μl N,N-diisopropylethylamine were added. After 15 min at 0° C. 86 mg amino-isobutyric acid methyl ester hydrochloride and 98 μl N,N-diisopropylethylamine were added and the reaction was stirred for 0.5 h at 0° C. and for 4 h at room temperature. Then, the reaction mixture was concentrated, the residue was taken up in ethyl acetate and washed with 2 M HCl, aqueous sat. sodium hydrogen carbonate solution and brine. The organic layer was dried over sodium sulphate, concentrated and purified by chromatography on silica (ethyl acetate/heptane) to yield 85 mg of a mixture of the (E)- and (Z)-isomers of 2-methyl-2-{[1-(4-phenyl-but-1-enyl)-naphthalene-2-carbonyl]-amino}-propionic acid methyl ester.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501981B2
Source datasetuspto-grants-2013_08
ORD IDord-d3e11eb8d73047d482054447d0e63880
Source noteuspto-grants-2013_08