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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251395Generated: October 30, 2026

Acetic Anhydride → 2-(2-Acetamino-phenylsulfanyl)-phenyl-{4(2-(2-acetoxyethoxy)ethyl]piperazin-1-yl}methanone

https://huagongshe.com/reaction/251395

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantEthyl AcetateHCID 8857—
ReactantQuetiapine, open ring-HCID 11338588—
Product2-(2-Acetamino-phenylsulfanyl)-phenyl-{4(2-(2-acetoxyethoxy)ethyl]piperazin-1-yl}methanoneHCID 11155984—

Reaction Steps

[2-(2-amino-phenylsulfanyl)-phenyl]-{4(2-(2-hydroxyethoxy)ethyl]piperazin-1-yl}methanone (10.7 g, 0.027 mol) was dissolved in ethyl acetate (50 ml) and triethylamine (7.4 ml) was added into reaction mixture. Acetic anhydride (7.6 ml, 0.081 mol) was slowly added to the reaction mixture at room temperature. After 4 h, the reaction mixture was evaporated to give a dark blue oil which was dissolved in ethyl acetate (50 ml) and washed with 2×25 ml saturated NaHCO3 solution and once with brine. The organic phase was evaporated to give a brown oil (10.9 g). The residue of [2-(2-acetamino-phenylsulfanyl)-phenyl-{4(2-(2-acetoxyethoxy)ethyl]-piperazin-1-yl}methanone was used further without purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863441B2
Source datasetuspto-grants-2011_01
ORD IDord-0a4aed533096481791fefbef47eebc41
Source noteuspto-grants-2011_01