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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 400365Generated: October 29, 2026

(2S,4R)-4-Hydroxypyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl ester → 1-(1,1-Dimethylethyl) 2-methyl (2S,4R)-4-(((4-bromo-1,3-dihydro-2H-isoindol-2-yl)carbonyl)oxy)-1,2-pyrrolidinedicarboxylate

https://huagongshe.com/reaction/400365

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S,4R)-4-Hydroxypyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-methyl esterHCID 2734883—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
Reactant4-BromoisoindoleHCID 54019998—
SolventDimethylacetamideHCID 31374—
Product1-(1,1-Dimethylethyl) 2-methyl (2S,4R)-4-(((4-bromo-1,3-dihydro-2H-isoindol-2-yl)carbonyl)oxy)-1,2-pyrrolidinedicarboxylateHCID 5346556679.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution containing 0.5 g of (2S,4R)-1-tert-butyl 2-methyl 4-hydroxypyrrolidine-1,2-dicarboxylate (2 mmol) in 5 mL of N,N-dimethylacetamide, was added 370 mg of carbonyl diimidazole (1.1 equiv.). The reaction was heated at 60° C. for 1 hr, then 400 mg of 4-bromoisoindole (2 mmol) was added. The reaction was continued at 60° C. overnight. After cooling down, the reaction mixture was extracted with 50 mL of EtOAc, and washed with water, brine, and dried over Na2SO4. After filtration and concentration, the residue was purified by flash column chromatography on silica gel using heptanes/EtOAc (v/v 5/2), giving white solid 745 mg (79%). LC-MS: m/z=369.2 (ES+, M+1-Boc).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741837B2
Source datasetuspto-grants-2014_06
ORD IDord-f5cbdbc5c43143789c91775b9e44d874
Source noteuspto-grants-2014_06