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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1889622Generated: October 30, 2026

Trifluoroacetic acid → N-(3-(Aminomethyl)benzyl)-3,5-dichloro-N-(4-(4-fluorophenoxy)benzyl)-2-hydroxybenzenesulfonamide

https://huagongshe.com/reaction/1889622

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-Butyl 3-((3,5-dichloro-N-(4-(4-fluorophenoxy)benzyl)-2-hydroxyphenylsulfonamido)methyl)benzylcarbamateHCID 58531654—
SolventDichloromethaneHCID 6344—
ProductN-(3-(Aminomethyl)benzyl)-3,5-dichloro-N-(4-(4-fluorophenoxy)benzyl)-2-hydroxybenzenesulfonamideHCID 5853135178.2%

Reaction Steps

To a solution of tert-butyl 3-((3,5-dichloro-N-(4-(4-fluorophenoxy)benzyl)-2-hydroxyphenylsulfonamido)methyl)benzylcarbamate (0.98 g, 1.48 mmol) in CH2Cl2 (15 mL) was added TFA (2.28 mL, 29.6 mmol). The reaction mixture was stirred at rt for 3 h. The mixture was concentrated and the residue was partitioned between ethyl acetate and saturated NaHCO3 solution. The organic layer (clear solution) was washed with brine, dried over MgSO4 and concentrated to give white solid (0.65 g, 70%). 1H NMR (DMSO-d6): δ 8.50 (bs, 1H), 7.52 (s, 1H), 7.34 (d, J=2.8 Hz, 1H), 7.2.9 (d, J=2.8 Hz, 1H), 7.26-7.21 (m, 4H), 7.12-7.08 (m, 3H), 6.97-6.94 (m, 2H), 6.80 (d, J=6.8 Hz, 2H), 4.41 (s, 2H), 4.32 (s, 2H), 3.94 (s, 2H); MS (ESI): (M+H)+=561.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08501992B2
Source datasetuspto-grants-2013_08
ORD IDord-c0ed4a51a3dc42369c3ad542f9ddc463
Source noteuspto-grants-2013_08