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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063824Generated: November 3, 2026

Triethylamine → (E)-4-[2-{2-[N-phenoxycarbonyl-N-(4-methoxybenzenesulfonyl)amino]phenyl}ethenyl]pyridine

https://huagongshe.com/reaction/1063824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPhenyl chloroformateHCID 15891—
ReactantHmn 154HCID 6366736—
SolventChloroformHCID 6212—
Product(E)-4-[2-{2-[N-phenoxycarbonyl-N-(4-methoxybenzenesulfonyl)amino]phenyl}ethenyl]pyridineHCID 12112542—

Reaction Steps

1.00 g of (E)-4-[2-{2-[N-(4-methoxybenzenesulfonyl)amino]phenyl}ethenyl]pyridine was suspended in 40 ml of chloroform and, after adding 1.82 g of phenyl chlorocarbonate, 1.20 g of triethylamine was slowly added under ice cooling. Then, the mixture was stirred at room temperature for 5 minutes. The solvent was distilled off under reduced pressure and the desired product was purified by silica gel column (carrier: Wako Gel C200, developing solvent chloroform) to obtain the desired compound. The desired compound was treated with ethanol to obtain 0.71 g of a white granular crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06967211B2
Source datasetuspto-grants-2005_11
ORD IDord-c9349e39a0d74faa949d4c24aa3e2e3d
Source noteuspto-grants-2005_11