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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1923997Generated: November 1, 2026

HCID 59366875, compound → HCID 59367253, compound

https://huagongshe.com/reaction/1923997

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 59366875HCID 59366875—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductHCID 59367253HCID 5936725386.4%

Reaction Steps

To a solution of tert-butyl N-[(1S)-4-(3-{[(benzyloxy)carbonyl]amino}pyrrolidin-1-yl)-1-{[(1R)-1-[(quinolin-3-yl)carbamoyl]-2-[4-(trifluoromethyl)phenyl]ethyl]carbamoyl}butyl]carbamate CXIII (170 mg, 0.22 mmol) in methanol (20 mL) was added catalytic amount of 10% Pd/C catalyst. The mixture was hydrogenated at normal pressure for 48 h. The catalyst was filtered through Celite and the filtrate was concentrated to give tert-butyl N-[(1S)-4-(3-aminopyrrolidin-1-yl)-1-{[(1R)-1-[(quinolin-3-yl)carbamoyl]-2-[4-(trifluoromethyl)phenyl]ethyl]carbamoyl}butyl]carbamate CXIV (120 mg, 0.19 mmol, 86.4% yield). ESIMS found for C33H41N6O4F3 m/z 643 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08178490B2
Source datasetuspto-grants-2012_05
ORD IDord-9e1e7ce9f3904132b6259ffd92faf1bc
Source noteuspto-grants-2012_05