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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927025Generated: October 26, 2026

Trifluoroacetic acid → 6-[[[1(R)-(4-chlorophenyl)ethyl]amino]carbonyl]-2-(4-fluorophenyl)-3-quinolinepentanoic acid

https://huagongshe.com/reaction/927025

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactant(1R)-1-(4-chlorophenyl)ethan-1-amineHCID 1715226—
Reactant2-Amino-5-bromobenzaldehydeHCID 23510475—
Reactant7-(4-Fluorophenyl)-7-oxoheptanoic acidHCID 24726875—
ReactantTFAA tBuOHHCID 86701127—
Product6-[[[1(R)-(4-chlorophenyl)ethyl]amino]carbonyl]-2-(4-fluorophenyl)-3-quinolinepentanoic acidHCID 67985852—

Reaction Steps

In a manner similar to that described previously (Example 1), 2-amino-5-bromobenzaldehyde was sequentially reacted with 7-(4-fluorophenyl)-7-oxoheptanoic acid and TFAA-tBuOH. The resulting ester 5B was converted to 5C (Pd(OAc)2, dcpp-2(HBF)4, K2CO3, 5 atm CO, H2O-DMF, 100° C. overnight), coupled with (R)-1-(4-chlorophenyl)ethanamine (HATU, DIPEA) and deprotected with TFA to provide the title compound, 6-[[[1(R)-(4-chlorophenyl)ethyl]amino]carbonyl]-2-(4-fluorophenyl)-3-quinolinepentanoic acid, 5. LCMS (M+H)=505.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09290453B2
Source datasetuspto-grants-2016_03
ORD IDord-59ea138ec912463b80940f2b28e1f598
Source noteuspto-grants-2016_03