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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514656Generated: November 1, 2026

Sodium Bicarbonate → HCID 66670255, compound

https://huagongshe.com/reaction/1514656

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantBoron tribromide dichloromethaneHCID 22277759—
ReactantHCID 66670261HCID 66670261—
SolventDichloromethaneHCID 6344—
ProductHCID 66670255HCID 66670255—

Reaction Steps

A 400 mg portion of N-(diaminomethylene)-1-[2-(4-fluorophenyl)ethyl]-5-(2-methoxyphenyl)-2-methyl-1H-pyrrole-3-carboxamide was dissolved in 10 ml of dichloromethane, and 3.04 ml of a 1 M boron tribromide dichloromethane solution was added dropwise thereto at −70° C. under an atmosphere of argon, followed by stirring at room temperature for 15 hours. Then, 100 ml of a saturated sodium bicarbonate aqueous solution was added to the reaction solution, followed by three times extractions with 20% methanol/chloroform. After drying the organic layer with anhydrous magnesium sulfate, the solvent was evaporated under a reduced pressure, and the residue was purified by silica gel column chromatography (Chromatorex (registered trademark), methanol:chloroform=10:90-20:80). Then, the resulting product was dissolved in 3 ml of ethyl acetate and, under ice-cooling, 0.132 ml of 4 M hydrogen chloride/ethyl acetate was added, followed by stirring overnight at room temperature. The resulting solid was collected by filtration to obtain 90 mg of N-(diaminomethylene)-1-[2-(4-fluorophenyl)ethyl]-5-(2-hydroxyphenyl)-2-methyl-1H-pyrrole-3-carboxamide hydrochloride as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222274B2
Source datasetuspto-grants-2012_07
ORD IDord-971edf9a0a4e485ab31e277bc7c6c208
Source noteuspto-grants-2012_07