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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2214810Generated: October 31, 2026

Hydrochloric Acid → HCID 69550750, compound

https://huagongshe.com/reaction/2214810

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 69550015HCID 69550015—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 69550750HCID 69550750—

Reaction Steps

Iodotrimethylsilane (2.51 ml) was added to a solution of 1-[4-benzyloxycarbonylamino-1-(4-pyridyl)-4-piperidylmethyl]-4-(6-chloronaphthalene-2-sulfonyl)-2-piperazinone (4.58 g) in dichloromethane (50 ml), and the mixture was stirred at room temperature for 4 hours. Methanol (10 ml) and 4N hydrochloric acid solution in ethyl acetate (8 ml) were added thereto. Methanol was added to obtain a solution, followed by concentration under reduced pressure. Dilute hydrochloric acid was added to the residue, and the mixture was washed with ether. The aqueous layer was made basic with 6N sodium hydroxide, followed by extraction with ethyl acetate. The organic layer was washed successively with an aqueous sodium bicarbonate solution and an aqueous saturated sodium chloride solution, dried, and concentrated. Dilute hydrochloric solution was added to the residue, which was purified by CHP20 column chromatography (water:acetonitrile:1N hydrochloric acid=100:0:1→80:20:1) to obtain the colorless amorphous title compound (3.66 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07109200B2
Source datasetuspto-grants-2006_09
ORD IDord-b4d79b17acc44b0a81147ae01c2355ae
Source noteuspto-grants-2006_09