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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357469Generated: November 2, 2026

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

https://huagongshe.com/reaction/2357469

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantChlorotrimethylsilaneHCID 6397—
Reactant3-(5-chloro-1H-indol-3-yl)piperidine-1-carboxylic acid-(4-dimethylamino-4-phenylcyclohexyl)-amideHCID 59385565—
SolventMethyl Ethyl KetoneHCID 6569—
Product3-(5-chloro-1H-indol-3-yl)piperidine-1-carboxylic acid-(4-dimethylamino-4-phenylcyclohexyl)-amideHCID 59385565—
Product3-(5-chloro-1H-indol-3-yl)piperidine-1-carboxylic acid-(4-dimethylamino-4-phenylcyclohexyl)-amide hydrochlorideHCID 67532661—

Reaction Steps

To prepare the hydrochloride the polar diastereoisomer of 3-(5-chloro-1H-indol-3-yl)piperidine-1-carboxylic acid-(4-dimethylamino-4-phenylcyclohexyl)-amide (86 mg, 0.18 mmole) was dissolved in ethyl methyl ketone (3 ml) and chlorotrimethylsilane (34 μl, 0.27 mmole) was added. The solid thereby formed was filtered off and dried. The hydrochloride of the polar diastereoisomer of 3-(5-chloro-1H-indol-3-yl)piperidine-1-carboxylic acid-(4-dimethylamino-4-phenylcyclohexyl)-amide was thereby obtained in a yield of 92 mg (100%) as a colourless solid (Example 36) with an m.p. of 158°-160° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759385B2
Source datasetuspto-grants-2010_07
ORD IDord-9c3468bb12b74f159696befb913fd031
Source noteuspto-grants-2010_07