Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1716681Generated: November 3, 2026

Trifluoroacetic acid → HCID 25261412, compound

https://huagongshe.com/reaction/1716681

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTriethylsilaneHCID 12052—
ReactantHCID 59831813HCID 59831813—
SolventDichloromethaneHCID 6344—
ProductHCID 25261412HCID 2526141271%

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 0° C. solution of [3-(1-Methanesulfonyl-1H-indol-5-yl)-3-phenyl-propyl]-methyl-carbamic acid tert-butyl ester LXXVI (56 mg, 0.127 mmol) in DCM (3 ml) was added triethylsilane (300 μl) and TFA (1.5 ml). The resulting mixture was stirred at 0° C. for 5 minutes and at room temperature for 40 minutes. The mixture was concentrated, and the residue was partitioned between a saturated solution of NaHCO3 and EtOAc. The combined organic layers were dried over Na2SO4, filtered, concentrated, and purified via flash chromatography (DCM/MeOH/NH4OH) affording [3-(1-Methanesulfonyl-1H-indol-5-yl)-3-phenyl-propyl]-methyl-amine LXXVIII as a white solid (31 mg, 71% yield). The amine LXXVIII (31 mg, 71% yield) was dissolved in Et2O (3 ml) and HCl (1M in Et2O, 95 μl) was added. The precipitate was filtered, washed with Et2O and dried in vacuo to afford the hydrochloride as a white powder (33 mg, 96% yield). MS (M+H)=343

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07803830B2
Source datasetuspto-grants-2010_09
ORD IDord-c0a2c90c7cb841eb925a1ebde39ae2e9
Source noteuspto-grants-2010_09