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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431886Generated: November 2, 2026

Diisopropylethylamine → (2S,5S)-1-tert-butyl 2-(3-chloro-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-9-yl) 5-methylpyrrolidine-1,2-dicarboxylate

https://huagongshe.com/reaction/1431886

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant(5S)-1-(tert-Butoxycarbonyl)-5-methyl-L-prolineHCID 15516206—
Reactant9-bromo-3-chloro-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-oneHCID 69673292—
SolventAcetonitrileHCID 6342—
SolventEthyl AcetateHCID 8857—
Product(2S,5S)-1-tert-butyl 2-(3-chloro-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-9-yl) 5-methylpyrrolidine-1,2-dicarboxylateHCID 6967557582.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a solution of 9-bromo-3-chloro-10,11-dihydro-5H-dibenzo[c,g]chromen-8(9H)-one (1.41 g, 3.88 mmol) in MeCN (17 mL) was added (2S,5S)-1-(tert-butoxycarbonyl)-5-methylpyrrolidine-2-carboxylic acid (980 mg, 4.27 mmol) and DIPEA (1.49 mL, 8.54 mmol). After stirring for 18 h at 50° C., the solution was diluted with EtOAc and washed successively with 1N HCl, saturated aqueous NaHCO3 and brine. The organics were dried over Na2SO4, filtered and concentrated under reduced pressure. The crude residue was purified by silica column chromatography (10% to 30% EtOAc/hexanes) to afford (2S,5S)-1-tert-butyl 2-(3-chloro-8-oxo-8,9,10,11-tetrahydro-5H-dibenzo[c,g]chromen-9-yl) 5-methylpyrrolidine-1,2-dicarboxylate (1.63 g, 81%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940718B2
Source datasetuspto-grants-2015_01
ORD IDord-9f8e50ee76f849558b6d0a52dc3045a4
Source noteuspto-grants-2015_01