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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1526423Generated: November 2, 2026

Ethylenediamine → (R)-2-(9-chloro-7-(4-isopropoxy-3-(trifluoromethyl)benzyloxy)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-yl)acetic acid ethylenediamine salt hydrate

https://huagongshe.com/reaction/1526423

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
ReactantAcetonitrileHCID 6342—
Reactant(R)-2-(9-chloro-7-(4-isopropoxy-3-(trifluoromethyl)benzyloxy)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-yl)acetic acidHCID 53362086—
SolventTetrahydrofuranHCID 8028—
Product(R)-2-(9-chloro-7-(4-isopropoxy-3-(trifluoromethyl)benzyloxy)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-yl)acetic acid ethylenediamine salt hydrateHCID 131733173—

Reaction Steps

(R)-2-(9-Chloro-7-(4-isopropoxy-3-(trifluoromethyl)benzyloxy)-2,3-dihydro-1H-pyrrolo[1,2-a]indol-1-yl)acetic acid (15 mg) was dissolved in THF (0.5 mL) and aqueous ethylenediamine (16 uL, 2.27 M) was added. The homogeneous solution was left to stir at room temperature for 2d. ACN (300 μL) was then added and the reaction was stirred at room temperature for one additional day. The reaction mixture was evaporated to dryness and 0.5 mL of EtOAc was added. After stiffing for 24 h at room temperature, a solid had formed which was collected by filtration. The PXRD pattern of the title compound is shown in FIG. 10; and the DSC and TGA are shown in FIG. 11.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085581B2
Source datasetuspto-grants-2015_07
ORD IDord-573e21a452624ed8acf5f1575512fa33
Source noteuspto-grants-2015_07