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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255030Generated: November 2, 2026

1-Hydroxybenzotriazole → HCID 59401203, compound

https://huagongshe.com/reaction/1255030

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Quinuclidinol, (-)-HCID 91404—
Reactant3-[(Carboxy-phenyl-methyl)-amino]-benzoic acid ethyl ester hydrochlorideHCID 67425851—
SolventTetrahydrofuranHCID 8028—
ProductHCID 59401203HCID 5940120379%

Reaction Steps

3-[(Carboxy-phenyl-methyl)-amino]-benzoic acid ethyl ester hydrochloride (I66) (161 mg, 0.48 mmol), 2-(1H-benzo[d][1,2,3]triazol-1-yl)-1,1,3,3-tetramethylisouronium hexafluorophosphate (V) (218 mg, 0.57 mmol), and HOBT (88 mg, 0.57 mmol) are dissolved in dry THF (10 mL). (R)-Quinuclidin-3-ol (61.0 mg, 0.48 mmol) and DIPEA (0.17 mL, 0.96 mmol) are added and the mixture is stirred under inert atmosphere overnight. THF is evaporated and the crude residue is dissolved in EtOAc and washed with sat. NaHCO3, water and brine. The recovered organic layer is dried (Na2SO4), filtered and evaporated. The crude is purified by flash chromatography (DCM/MeOH=95/5) to afford the title compound as a yellow oil (154 mg, 79% yield, mixture of diastereoisomers).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455646B2
Source datasetuspto-grants-2013_06
ORD IDord-75c36abc776544e7af39fee7dd2bdce7
Source noteuspto-grants-2013_06