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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273869Generated: October 31, 2026

Trifluoroacetic acid → HCID 53713896, compound

https://huagongshe.com/reaction/273869

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 53774142HCID 53774142—
SolventDichloromethaneHCID 6344—
ProductHCID 53713896HCID 5371389686.6%

Reaction Steps

To a solution of (R)-(-)-1-(4-benzyloxybutyl)-5-[2-[N-tert-butoxycarbonyl-2-[2-(2,2,2-trifluoroethoxy)phenoxy]ethylamino]propyl]indoline-7-carboxamide (523 mg) in methylene chloride (7.5 ml) was added dropwise trifluoroacetic acid (1.5 ml) with stirring under ice cooling, and the mixture was stirred at room temperature for 4 hours. To the reaction mixture was added a saturated aqueous sodium bicarbonate solution, and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by medium pressure liquid column chromatography on silica gel using a mixture of chloroform and methanol (10/1) as eluent to give 388 mg of (R)-(-)-1-(4-benzyloxybutyl)-5-[2-[2-[2-(2,2,2-trifluoroethoxy)phenoxy]ethylamino]propyl]indoline-7-carboxamide melting at 101°-102° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05387603
Source datasetuspto-grants-1995_02
ORD IDord-6fc42638b9a94356afe2ce93766013f4
Source noteuspto-grants-1995_02