Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2279517Generated: October 31, 2026

Phthalimide → HCID 86705515, compound

https://huagongshe.com/reaction/2279517

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhthalimideHCID 6809—
Reactant4-Bromo-1,2-dichlorobenzeneHCID 29013—
Reactant(2R)-1-[(tert-butoxy)carbonyl]pyrrolidine-2-carboxylic acidHCID 688022—
Reactant(R)-2-Methyl-CBS-oxazaborolidineHCID 9838490—
ReactantHCID 86705516HCID 86705516—
ProductHCID 86705515HCID 86705515—

Reaction Steps

(R)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid and be converted to (R)-tert-butyl 2-(3,4-dichlorobenzoyl)-pyrrolidine-1-carboxylate in accord with steps 1 and 2 of example 11, except in step 2,4-bromo-1-(trifluoromethyl)benzene was replaced with 1-bromo-3,4-dichlorobenzene. Reduction of the ketone with (R)-1-methyl-3,3-diphenylhexahydropyrrolo[1,2-c][1,3,2]oxazaborole and condensation with isoindoline-1,3 dione can be carried out in accord with procedures in steps 4 and 5 of example 11 to afford (R)-tert-butyl 2-((S)-(3,4-dichlorophenyl)(1,3-dioxoisoindolin-2-yl)methyl)pyrrolidine-1-carboxylate (242).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133187B2
Source datasetuspto-grants-2015_09
ORD IDord-25f732db103d4b029c62625ae5bf31fc
Source noteuspto-grants-2015_09