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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255022Generated: November 1, 2026

1-Hydroxybenzotriazole → HCID 46840706, compound

https://huagongshe.com/reaction/1255022

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Quinuclidinol, (-)-HCID 91404—
Reactant(3-Fluoro-4-methyl-phenylamino)-phenyl-acetic acid hydrochlorideHCID 67425700—
SolventAcetonitrileHCID 6342—
ProductHCID 46840706HCID 46840706100.5%

Reaction Steps

(3-Fluoro-4-methyl-phenylamino)-phenyl-acetic acid hydrochloride (I48) (250 mg, 0.84 mmol), 2-(1H-benzo[d][1,2,3]triazol-1-yl)-1,1,3,3-tetramethylisouronium hexafluorophosphate (V) (321 mg, 0.84 mmol), and HOBT (129 mg, 0.84 mmol) are dissolved in acetonitrile (6 mL). DIPEA (0.29 mL, 1.69 mmol) is added, followed by (R)-quinuclidin-3-ol (215 mg, 1.69 mmol) and the resulting yellow solution is stirred at RT overnight (Conversion complete by UPLC/MS-UV). MeCN is evaporated, the residue is dissolved in EtOAc and washed with sat. NaHCO3, water and brine. The organic layer is recovered, dried over Na2SO4, filtered and evaporated. The crude compound is purified by filtration through a pad of silica using DCM/MeOH=9/1 as the eluent to obtain the title compound as a yellow oil (311 mg, quantitative yield, mixture of diastereoisomers).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08455646B2
Source datasetuspto-grants-2013_06
ORD IDord-8d5535bbfcf749c58ff47c000af01c0a
Source noteuspto-grants-2013_06