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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | 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 | HCID 67391526 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-Cyclopropyl-3-fluoro-5-[2-{[1-(hydroxymethyl)cyclobutyl]methyl}-1-oxo-4-(piperazin-1-ylmethyl)-1,2-dihydroisoquinolin-6-yl]-4-methylbenzamide | HCID 59285277 | 31.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08012980B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-a7a443d2a4a641c4b73eff4ace06667b |
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| Source note | uspto-grants-2011_09 |
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