Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2041752Generated: November 2, 2026

Trifluoroacetic acid → HCID 68161452, compound

https://huagongshe.com/reaction/2041752

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 68184862HCID 68184862—
SolventDichloromethaneHCID 6344—
ProductHCID 68161452HCID 6816145283%

Reaction Steps

A solution of 1,1-dimethylethyl (2-{4-[(2S,4R)-1-acetyl-2-methyl-4-(2-pyridinylamino)-1,2,3,4-tetrahydro-6-quinolinyl]-1H-pyrazol-1-yl}ethyl)methylcarbamate (for a preparation see intermediate 60) (126 mg, 0.250 mmol) in dichloromethane (DCM) (2 mL) was treated at room temperature with trifluoroacetic acid (TFA) (500 μl, 6.49 mmol) and the resulting mixture was stirred at this temperature for 1.5 h then concentrated in vacuo. The residue was dissolved in MeOH (1 mL) and purified by MDAP (modifier: formic acid). The desired fractions were combined and the solvent was removed under vacuo to give (2S,4R)-1-acetyl-2-methyl-6-{1-[2-(methylamino)ethyl]-1H-pyrazol-4-yl}-N-2-pyridinyl-1,2,3,4-tetrahydro-4-quinolinamine formate (93 mg, 0.206 mmol, 83% yield) as a cream solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08580957B2
Source datasetuspto-grants-2013_11
ORD IDord-d6127b2311784e99ac39b76e33eb3826
Source noteuspto-grants-2013_11