Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1527378Generated: November 4, 2026

(2S,4R)-1-(1-carbamoyl-1H-indol-3-ylcarbamoyl)-4-fluoro-pyrrolidine-2-carboxylic acid benzyl ester → (2S,4R)-1-(1-Carbamoyl-1H-indol-3-ylcarbamoyl)-4-fluoro-pyrrolidine-2-carboxylic acid

https://huagongshe.com/reaction/1527378

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2S,4R)-1-(1-carbamoyl-1H-indol-3-ylcarbamoyl)-4-fluoro-pyrrolidine-2-carboxylic acid benzyl esterHCID 68283894—
CatalystPalladiumHCID 23938—
SolventTetrahydrofuranHCID 8028—
Product(2S,4R)-1-(1-Carbamoyl-1H-indol-3-ylcarbamoyl)-4-fluoro-pyrrolidine-2-carboxylic acidHCID 68284228—

Reaction Steps

To a solution of (2S,4R)-1-(1-carbamoyl-1H-indol-3-ylcarbamoyl)-4-fluoro-pyrrolidine-2-carboxylic acid benzyl ester (2.5 g, 5.89 mmol) in THF (40 mL) was added Pd/C 10% (500 mg). Air was removed from the flask under high vacuum and replaced with nitrogen, this operation was repeated three times and finally nitrogen was removed and replaced with hydrogen. The mixture was stirred under a hydrogen atmosphere for 16 h. Hydrogen was removed under vacuum and replaced with nitrogen and the catalyst was removed by filtration over a pad of Celite and washed with THF. Solvents were concentrated to give the title product. MS (LC/MS): 335.0 [M+H]+, 691.2 [2M+Na]+, 333.1 [M−H]−; tR (HPLC conditions a): 2.22 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09085555B2
Source datasetuspto-grants-2015_07
ORD IDord-8caf71949da14e12b675730c2e307b7a
Source noteuspto-grants-2015_07