HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2426082Generated: November 1, 2026
Trifluoroacetic acid → HCID 67147452, compound
https://huagongshe.com/reaction/2426082
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 58707252 | HCID 58707252 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 67147452 | HCID 67147452 | 59% |
Reaction Steps
A mixture of tert-butyl 4-(3-(3,5-dichlorobenzylamino)-4-(methylsulfonyl)phenyl)-piperazine-1-carboxylate (0.5 mmol), trifluoroacetic acid (5 mL) and dichloromethane (10 mL) was stirred for 3 h and concentrated in vacuo. The residue was dissolved in dichloromethane; this solution was washed with aqueous NaHCO3 solution, dried over Na2SO4 and concentrated in vacuo. The yellow solid residue was dissolved in dichloromethane (1 mL), reacted with 1 N HCl in ether (1 mL) and concentrated in vacuo to yield the title compound as a yellow solid (59%). 1H NMR (400 MHz, CDCl3): δ 9.37 (br, 1H), 7.62 (d, 1H), 7.28 (s, 1H), 7.22 (s, 2H), 6.24 (dd, 1H), 5.71 (d, 1H), 4.43 (d, 2H), 3.30 (m, 4H), 2.93 (m, 4H). MS (ESI) m/z: Calculated: 450.81; Observed: 415.4 (M+H+ corresponding to its free base).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07968538B2 |
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| Source dataset | uspto-grants-2011_06 |
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| ORD ID | ord-0e1a1cc7e185417e9d03cdd9c2c91a7a |
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| Source note | uspto-grants-2011_06 |
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