Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1666869Generated: October 26, 2026

Sodium Sulfate → N-(2-(4,5,6,7-Tetrafluoro-1H-indol-3-yl)ethyl)-3-(2,2,2-trifluoroethoxy)benzylamine

https://huagongshe.com/reaction/1666869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium SulfateHCID 24436—
Reactant3-(2,2,2-Trifluoroethoxy)benzaldehydeHCID 4770947—
ReactantHCID 15584731HCID 15584731—
SolventEthanolHCID 702—
ProductN-(2-(4,5,6,7-Tetrafluoro-1H-indol-3-yl)ethyl)-3-(2,2,2-trifluoroethoxy)benzylamineHCID 21071624—

Reaction Steps

By a method similar to Example 763, using 2-(4,5,6,7-tetrafluoro-1H-indol-3-yl)ethylamine (484 mg, 2.08 mmol), ethanol (45 mL), 3-(2,2,2-trifluoroethoxy)benzaldehyde (425 mg, 2.08 mmol), anhydrous sodium sulfate (3.5 g) sodium borohydride (236 mg, 6.24 mmol) to give the free base of the title compound as a straw colored solid. Recrystallize from methylene chloride to obtain the title compound: mp 107.2-108.2° C. 1H NMR (400 MHz, dmso-d6): 11.92 (br s, 1H), 7.32 (s, 2H), 6.95-6.99 (m, 2H), 6.87 (dd, 1H, J=2.4, 8.0 Hz) 4.68 (q, 2H, J=8.8 Hz), 3.70 (s, 2H), 2.88 (t, 2H, J=7.2 Hz) 2.75 (t, 2H, J=7.2 Hz). MS (ES+): m/e 421.1 (M+1). CHN (for C19H15F7N2O.1HCl.0.20H2O) calcd: C, 53.83; H, 3.66; N, 6.61. found: C, 53.75; H, 3.33; N, 6.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08044090B2
Source datasetuspto-grants-2011_10
ORD IDord-2aabd7ba6ac74eaeb7a8e2b50bb7a1a3
Source noteuspto-grants-2011_10