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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 469470Generated: October 30, 2026

Dicyclohexylcarbodiimide → (R)-quinuclidin-3-yl 2-(benzo[b]thiophen-7-yl)-2-(phenylamino)acetate

https://huagongshe.com/reaction/469470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant3-Quinuclidinol, (-)-HCID 91404—
Reactant2-(Benzo[b]thiophen-7-yl)-2-(phenylamino)acetic acidHCID 58557038—
SolventTetrahydrofuranHCID 8028—
Product(R)-quinuclidin-3-yl 2-(benzo[b]thiophen-7-yl)-2-(phenylamino)acetateHCID 5855700342.9%

Reaction Steps

A mixture of 2-(benzo[b]thiophen-7-yl)-2-(phenylamino)acetic acid (I26) (303 mg, 1.07 mmol), (R)-quinuclidin-3-ol (136 mg, 1.07 mmol), DCC (221 mg, 1.07 mmol) and HOBT (164 mg, 1.07 mmol) in THF (20 ml) was stirred at r.t. for three days. THF was evaporated, and the crude product was taken up with EtOAc and washed twice with 2M K2CO3, and then with brine. The organic phase was dried over Na2SO4, filtered and evaporated to dryness. The crude was purified by flash chromatography (EtOAc/MeOH=9/1 to EtOAc/MeOH=9/1+0.5% NH4OH) to obtain (R)-quinuclidin-3-yl 2-(benzo[b]thiophen-7-yl)-2-(phenylamino)acetate (180 mg, 42.9% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08629160B2
Source datasetuspto-grants-2014_01
ORD IDord-fdb1ceb0205f43978a4758de33e9a484
Source noteuspto-grants-2014_01