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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 554357Generated: October 29, 2026

Water → tert-Butyl [(1-{[3-(aminocarbonyl)phenyl]sulfonyl}-5-phenyl-1H-pyrrol-3-yl)methyl]methylcarbamate

https://huagongshe.com/reaction/554357

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole, ammonium saltHCID 22033809—
Reactant3-[(4-{[(tert-Butoxycarbonyl)(methyl)amino]methyl}-2-phenyl-1H-pyrrol-1-yl)sulfonyl]benzoic acidHCID 66924990—
SolventDimethylformamideHCID 6228—
Producttert-Butyl [(1-{[3-(aminocarbonyl)phenyl]sulfonyl}-5-phenyl-1H-pyrrol-3-yl)methyl]methylcarbamateHCID 6692519294.3%

Reaction Steps

To a solution (5 mL) of 3-[(4-{[(tert-butoxycarbonyl)(methyl)amino]methyl}-2-phenyl-1H-pyrrol-1-yl)sulfonyl]benzoic acid (205 mg) in N,N-dimethylformamide were added 1-ethyl-3-(3-dimethylaminopropyl)-carbodiimide hydrochloride (125 mg) and 1-hydroxy-1H-benzotriazole ammonium salt (100 mg) at room temperature. The mixture was stirred at the same temperature for 1 hr, water was added and the mixture was extracted with ethyl acetate. The extract was washed with water and saturated brine, dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (eluent: hexane-ethyl acetate=4:1→1:1→1:4) to give the title compound as a colorless oil (yield 193 mg, 94%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08048909B2
Source datasetuspto-grants-2011_11
ORD IDord-d9c6ee3469ba4e75a2dcfb40aa906e0b
Source noteuspto-grants-2011_11