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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1163095Generated: October 28, 2026

Acetonitrile → (3'S)-1'-[4-(1H-indol-1-ylmethyl)benzoyl]-1,3'-bipyrrolidine

https://huagongshe.com/reaction/1163095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantCarbodiimideHCID 160435—
Reactant(3S)-3-(Pyrrolidin-1-YL)pyrrolidineHCID 7176274—
Reactant4-((1H-indol-3-yl)methyl)benzoic acidHCID 68425742—
SolventTriethylamineHCID 8471—
Product(3'S)-1'-[4-(1H-indol-1-ylmethyl)benzoyl]-1,3'-bipyrrolidineHCID 46230691—

Reaction Steps

A solution of methyl 4-((1H-indol-3-yl)methyl)benzoate (Tet. Lett. 44 (2003) 4589-4591) (0.50 g, 1.88-mmol) in methanol is treated with an aqueous solution of NaOH (4.15 mL, 1N, 4.15 mmol), heated to reflux temperature for 3 h and concentrated in vacuo. The resultant solid residue is dissolved in H2O and acidified with HCl. The resultant precipitate is removed by filtration and dried to yield 4-((1H-indol-3-yl)methyl)benzoic acid as a white solid, 0.468 g (99%). A microwave vial is charged with PS-Carbodiimide (0.275 g, 1.2 mmol/g, 0.33 mmol). To the vial is added a solution of 4-((1H-indol-3-yl)methyl)-benzoic acid (0.070 g, 0.28 mmol) in CH3CN, a solution of HOBT (0.045 g, 0.33 mmol) in CH3CN, a solution of (S)-1,3′-bipyrrolidine (0.065 g, 0.31 mmol) in CH3CN and 0.11 mL of triethylamine. The reaction mixture is irradiated in the Emry's Optimizer at 110° C. for 6 minutes and then concentrated under reduced pressure. The resultant residue is purified by flash chromatography to yield the title product as a white solid, 0.064 g, (68%), mp 141-153° C., identified by H1 NMR and mass spectral analyses. MS (ES) m/z 372.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820825B2
Source datasetuspto-grants-2010_10
ORD IDord-7fc68efac2f4481a99f25bca242a1106
Source noteuspto-grants-2010_10