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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357478Generated: November 1, 2026

Hydrochloric Acid → 3-(5-fluoro-1H-indol-3-yl)piperidine-1-carboxylic acid-(4-dimethylamino-4-phenylcyclohexyl)-amide

https://huagongshe.com/reaction/2357478

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChlorotrimethylsilaneHCID 6397—
Reactant3-(5-fluoro-1H-indol-3-yl)piperidine-1-carboxylic acid-(4-dimethylamino-4-phenylcyclohexyl)-amideHCID 59385567—
SolventMethyl Ethyl KetoneHCID 6569—
Product3-(5-fluoro-1H-indol-3-yl)piperidine-1-carboxylic acid-(4-dimethylamino-4-phenylcyclohexyl)-amideHCID 59385567—
Product3-(5-fluoro-1H-indol-3-yl)piperidine-1-carboxylic acid-(4-dimethylamino-4-phenylcyclohexyl)-amide hydrochlorideHCID 67533414—

Reaction Steps

To prepare the hydrochloride the polar diastereoisomer of 3-(5-fluoro-1H-indol-3-yl)piperidine-1-carboxylic acid-(4-dimethylamino-4-phenylcyclohexyl)-amide (200 mg, 0.43 mmole) was dissolved in ethyl methyl ketone (5 ml) and chlorotrimethylsilane (82 μl, 0.65 mmole) was added. The solid thereby formed was filtered off and dried. The hydrochloride of the polar diastereoisomer of 3-(5-fluoro-1H-indol-3-yl)piperidine-1-carboxylic acid-(4-dimethylamino-4-phenylcyclohexyl)-amide was thereby obtained as a colourless solid with an m.p. of 160°-164° C. in a yield of 215 mg (100%) (Example 42).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759385B2
Source datasetuspto-grants-2010_07
ORD IDord-0e40b4c76a294f4dbbd6dabdd465ec91
Source noteuspto-grants-2010_07