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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 906429Generated: October 30, 2026

Trifluoroacetic acid → N-Cyclopropyl-3-fluoro-5-[2-{[1-(hydroxymethyl)cyclobutyl]methyl}-1-oxo-4-(piperazin-1-ylmethyl)-1,2-dihydroisoquinolin-6-yl]-4-methylbenzamide

https://huagongshe.com/reaction/906429

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTert-butyl 4-[(2-{[1-({[tert-butyl(dimethyl)silyl]oxy}methyl)cyclobutyl]methyl}-6-[5-(cyclopropylcarbamoyl)-3-fluoro-2-methylphenyl]-1-oxo-1,2-dihydroisoquinolin-4-yl)methyl]piperazine-1-carboxylateHCID 67391526—
SolventDichloromethaneHCID 6344—
ProductN-Cyclopropyl-3-fluoro-5-[2-{[1-(hydroxymethyl)cyclobutyl]methyl}-1-oxo-4-(piperazin-1-ylmethyl)-1,2-dihydroisoquinolin-6-yl]-4-methylbenzamideHCID 5928527731.2%

Reaction Steps

Trifluoroacetic Acid (3 mL, 38.94 mmol) was added to a solution of tert-butyl 4-[(2-{[1-({[tert-butyl(dimethyl)silyl]oxy}methyl)cyclobutyl]methyl}-6-[5-(cyclopropylcarbamoyl)-3-fluoro-2-methylphenyl]-1-oxo-1,2-dihydroisoquinolin-4-yl)methyl]piperazine-1-carboxylate (Example 27d 0.099 g) in DCM (9 mL) at room temperature. The reaction was stirred for 30 min before azeotroping with toluene (3×10 mL). The residue was passed through SCX resin, eluting with methanol to remove impurities, and then ˜0.7 N methanolic ammonia to elute product, which was then purified by preparative HPLC (Sunfire column using a 95-30% gradient of 0.3% aqueous ammonia in acetonitrile as eluent). The solvents were removed and the residue triturated with diethyl ether to leave the title compound (0.022 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08012980B2
Source datasetuspto-grants-2011_09
ORD IDord-a7a443d2a4a641c4b73eff4ace06667b
Source noteuspto-grants-2011_09