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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1010568Generated: October 31, 2026

Citric Acid → HCID 86618515, compound

https://huagongshe.com/reaction/1010568

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
Reactant(3S,4S)-3-(Boc-amino)-4-methylpyrrolidineHCID 11138119—
ReactantEthyl 2,4,5-trifluoro-3-methylbenzoateHCID 21220461—
SolventDimethyl SulfoxideHCID 679—
ProductHCID 86618515HCID 8661851570.2%

Reaction Steps

A solution of (3S,4S)-3-(tert-butoxycarbonyl)amino-4-methylpyrrolidine (1.80 g, 8.97 mmol), ethyl 3-methyl-2,4,5-trifluorobenzoate (2.18 g, 10.0 mmol), and 1,8-diazabicyclo[5.4.0]undeca-7-ene (DBU) (2.24 mL, 15 mmol) in dimethyl sulfoxide (20 mL) was stirred under a nitrogen atmosphere at an external temperature of 60° C. for 70 hours. The temperature of the mixture was cooled to room temperature. The resultant mixture was poured to a 10% aqueous citric acid solution, followed by extraction with ethyl acetate (200 mL×3), washing by water (200 mL), saturated aqueous sodium hydrogencarbonate (150 mL), and saturated brine (150 mL), and dried over anhydrous sodium magnesium. After filtration, the filtrate was concentrated under reduced pressure. The obtained residue was purified through silica gel column chromatography (n-hexane:ethyl acetate=6:1), to thereby yield the title compound as colorless crystals (2.51 g, 70.2%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07977327B2
Source datasetuspto-grants-2011_07
ORD IDord-86c0637d4c04490caebdbf39cd6d30ae
Source noteuspto-grants-2011_07