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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1814631Generated: November 2, 2026

1-Hydroxybenzotriazole → HCID 178500824, compound

https://huagongshe.com/reaction/1814631

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl beta-alanateHCID 192794—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 178453065HCID 178453065—
SolventDimethylformamideHCID 6228—
ProductHCID 178500824HCID 178500824—

Reaction Conditions

Temperature20 °C

Reaction Steps

Trans-4-{[N-(tert-butoxycarbonyl)-N-(4-tert-butylcyclohexyl)amino]methyl}benzoic acid (22.0 g, 56.5 mmol) and 1-hydroxybenzotriazole (8.6 g, 57.0 mmol, containing 12% w/w water) was dissolved in DMF (300 mL). N-Dimethylaminopropyl-N′-ethylcarbodiimide hydrochloride (10.9 g, 56.8 mmol), β-alanine methyl ester (8.4 g, 60 mmol) and diisopropylethylamine (25 mL, 142 mmol) were added and the clear solution stirred at 20° C. for 16 hours. Solvent was removed by rotary evaporation and the residual oil re-dissolved in ethyl acetate (500 mL). The organic phase was washed with 5% aqueous sodium hydrogen carbonate solution (2×500 mL), 0.5 M citric acid (2×250 mL) and brine before being dried with anhydrous Na2SO4. Solvent was removed and the residual oil evaporated twice from acetonitrile. The oil was used without further purification. Yield: 24.0 g (89%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06875760B2
Source datasetuspto-grants-2005_04
ORD IDord-ba167cd03f8744f8af631f0a91197d4f
Source noteuspto-grants-2005_04