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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633983Generated: October 31, 2026

Diisopropylethylamine → HCID 23550119, compound

https://huagongshe.com/reaction/1633983

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant3-Fluoro-5-(trifluoromethyl)benzoyl chlorideHCID 519364—
ReactantSpiro[5.5]undecan-3-oneHCID 574172—
ReactantHCID 22502126HCID 22502126—
ReactantHCID 23550130HCID 23550130—
SolventAcetonitrileHCID 6342—
ProductHCID 23550119HCID 23550119200.2%
ProductHCID 23550130HCID 23550130—

Reaction Steps

3-[4-(Spiro[5.5]undec-3-ylaminomethyl)benzoylamino]propionic acid ethyl ester was prepared by reductive alkylation of 3-(4-aminomethyl-benzoylamino)propionic acid ethyl ester with spiro[5.5]undecan-3-one. 3-[4-(Spiro[5.5]undec-3-ylaminomethyl)benzoylamino]propionic acid ethyl ester (200 mg, 499 μmol) was dissolved in acetonitrile (5 mL) and diisopropylethylamine (170 μL) and cooled on an ice bath. Commercially available 3-fluoro-5-(trifluoromethyl)benzoylchloride (136 mg, 602 μmol) dissolved in acetonitrile (5 mL) was added dropwise. The reaction was complete within one hour as shown by HPLC. The solvent was evaporated and water (10 mL) was added to the residue followed by saturated sodium bicarbonate (10 mL). The product was extracted using ethyl acetate (2×50 mL). The combined ethyl acetate extracts were washed with water (20 mL) and brine (20 mL). Drying the organic phases over MgSO4 and evaporation of the solvent afforded 3-(4-{[(3-fluoro-5-trifluoromethylbenzoyl)spiro[5.5]undec-3-yl-amino]methyl}benzoylamino)propionic acid ethyl ester (295 mg) which was hydrolyzed using sodium hydroxide to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06503949B1
Source datasetuspto-grants-2003_01
ORD IDord-36acbe65aa544c41b05255565d33e7c7
Source noteuspto-grants-2003_01