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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195677Generated: October 31, 2026

Oxalyl chloride → 4-[2-(Benzofurazan-5-yl)ethyl]-1-(indole-5-carbonyl)piperazine

https://huagongshe.com/reaction/1195677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
Reactant1H-Indole-5-Carboxylic AcidHCID 74280—
ReactantDiisopropylethylamineHCID 81531—
Reactant5-(2-Piperazin-1-ylethyl)-2,1,3-benzoxadiazoleHCID 15166382—
CatalystDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
Product4-[2-(Benzofurazan-5-yl)ethyl]-1-(indole-5-carbonyl)piperazineHCID 15166395—

Reaction Steps

Indole-5-carboxylic acid (57 mg, 0.35 mmol) was dissolved in THF (2 ml) and DMF (1 drop), then oxalyl chloride (37 μl, 54 mg, 0.42 mmol) was added. The mixture was stirred at room temperature for 3 hours, the solvent was evaporated under reduced pressure and the residue was dissolved in DMF (2 ml) and added to a stirred solution of 1-[2-(benzofurazan-5-yl)ethyl]piperazine (81 mg, 0.35 mmol) and diisopropylethylamine (91 μl, 68 mg, 0.52 mmol) in dichloromethane (1 ml). The mixture was stirred at room temperature for 24 hours, then the solvent was evaporated under reduced pressure. The residue was purified by flash column chromatography on silica gel, eluting with CH2Cl2 /CH3OH/NH3 ; 96:4:0.4 and crystallized from ethyl acetate/CHCl3 /hexane to give the piperazine as yellow microcrystals (16 mg, 12%), mp 180°-183° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112824
Source datasetuspto-grants-1992_05
ORD IDord-c929f49f7a3c4bd08781344c509356af
Source noteuspto-grants-1992_05