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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 736793Generated: October 29, 2026

Trifluoroacetic acid → HCID 86607894, compound

https://huagongshe.com/reaction/736793

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 86607893HCID 86607893—
SolventDichloromethaneHCID 6344—
ProductHCID 86607894HCID 86607894137.2%

Reaction Steps

To a solution of tert-butyl (3R,4R)-3-[(tert-butoxyamino)carbonyl]-3-hydroxy-4-[({4-[(2-methylquinolin-4-yl)methoxy]phenyl}sulfonyl)amino]piperidine-1-carboxylate (740 mg, 1.15 mmol) in CH2Cl2 (10 mL) was added trifluoroacetic acid (2.5 mL). The reaction was stirred at room temperature for 1.5 h. The solvent was concentrated in vacuo and methanol was used to chase residual trifluoroacetic acid. The residue was precipitated from ether as a white solid to yield 856 mg (97%) of (3R,4R)-N-tert-butoxy-3-hydroxy-4-(4-((2-methylquinolin-4-yl) methoxy)phenylsulfonamido)piperidine-3-carboxamide as the trifluoroacetic acid salt. MS: (M+H)+=543.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07595327B2
Source datasetuspto-grants-2009_09
ORD IDord-e097bfa873ba49b587df60d98d986770
Source noteuspto-grants-2009_09