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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2238996Generated: November 1, 2026

Citric Acid → HCID 67486828, compound

https://huagongshe.com/reaction/2238996

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 numberUS07718798B2
Source datasetuspto-grants-2010_05
ORD IDord-58bfe226f93241edb96ebd34e8e25b9a
Source noteuspto-grants-2010_05