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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1960393Generated: November 1, 2026

Citric Acid → HCID 67486828, compound

https://huagongshe.com/reaction/1960393

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantSodium BicarbonateHCID 516892—
Reactant1-(Methylsulfonyl)piperazineHCID 709161—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 86619906HCID 86619906—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 67486828HCID 6748682879.2%

Reaction Steps

A mixture of N-[2-(benzylthio)-3-oxopropyl]-7-[methyl(pyridin-2-ylsulfonyl)amino]-5-[3-(methylsulfonyl)propoxy]-1H-indole-2-carboxamide (0.35 g), N-methylsulfonylpiperazine (0.18 g) and 1,2-dichloroethane (8 mL) was stirred at room temperature for 20 min. Sodium triacetoxyborohydride (345 mg) was added to the reaction solution, and the mixture was stirred at room temperature for 16 hr. The reaction solution was acidified with aqueous citric acid solution, and basified with aqueous sodium hydrogencarbonate solution. The precipitated crystals were collected by filtration, washed with water and ethyl acetate, and dried to give the title compound (341 mg, yield: 43%) as colorless crystals. MS: 794(MH+). melting point: 195-196° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08410087B2
Source datasetuspto-grants-2013_04
ORD IDord-7b87f06c3d1a45fa9f4cf9862d32a69f
Source noteuspto-grants-2013_04