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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1673537Generated: October 25, 2026

Hydrochloric Acid → tert-butyl 4-phenyl-2-(4-(1H-pyrrol-1-yl)benzamido)benzoate

https://huagongshe.com/reaction/1673537

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantOxalyl chlorideHCID 65578—
Reactant4-(1H-Pyrrol-1-yl)benzoic acidHCID 2737256—
ReactantTert-butyl 3-amino-[1,1'-biphenyl]-4-carboxylateHCID 58508425—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
SolventEthyl AcetateHCID 8857—
Producttert-butyl 4-phenyl-2-(4-(1H-pyrrol-1-yl)benzamido)benzoateHCID 67344178—

Reaction Steps

0.015 mL of N,N-dimethylformamide was added to a mixed solution of 2.0 mL of methylene chloride and 0.024 mL of oxalyl chloride containing 47 mg of 4-(1H-pyrrol-1-yl)benzoic acid and stirred at room temperature for 30 minutes. 67 mg of tert-butyl 2-amino-4-phenylbenzoate and 0.090 mL of triethylamine were added to the reaction mixture at room temperature sequentially and stirred at the same temperature for 30 minutes. Ethyl acetate and 1.0 mol/L hydrochloric acid were added to the reaction mixture. The organic layer was separated and dried over anhydrous magnesium sulfate after washed with a saturated sodium chloride aqueous solution, and the solvent was evaporated under reduced pressure. The obtained residue was purified with silica gel column chromatography [PSQ100B (spherical) manufactured by Fuji Silysia Chemical Ltd., eluent; chloroform] to obtain 64 mg of tert-butyl 4-phenyl-2-(4-(1H-pyrrol-1-yl)benzamido)benzoate as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07999132B2
Source datasetuspto-grants-2011_08
ORD IDord-9672b81898db434793a1112ed4716ce0
Source noteuspto-grants-2011_08