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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2090597Generated: November 2, 2026

Trifluoroacetic acid → HCID 58246486, compound

https://huagongshe.com/reaction/2090597

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 58246455HCID 58246455—
SolventDichloromethaneHCID 6344—
ProductHCID 58246486HCID 58246486—

Reaction Steps

250 mg (0.42 mmol) of tert-butyl ((S)-1-(3H-imidazol-4-ylmethyl)-2-oxo-2-{4-[4-(5,5,8,8-tetramethyl-5,6,7,8-tetrahydronaphthalen-2-yl)thiazol-2-yl]-piperidin-1-yl}ethyl)carbamate are dissolved in 20 ml of dichloromethane and 1 ml of trifluoroacetic acid and stirred at room temperature for 12 h. The reaction mixture is washed with 0.1 N NaOH, the organic phase is dried over sodium sulfate and purified by column chromatography on silica gel. The crude product is dissolved in acetone, and a pH of 4 is set using 1 N HCl. A white precipitate forms in the process, which is filtered off with suction, washed with ether and dried in vacuo. Yield: 200 mg of “A63” hydrochloride, white solid; ESI: 492 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436186B2
Source datasetuspto-grants-2013_05
ORD IDord-e616cfc68cf74ee1b07cb0d64709ed01
Source noteuspto-grants-2013_05