HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → 2-(2-Acetamino-phenylsulfanyl)-phenyl-{4(2-(2-acetoxyethoxy)ethyl]piperazin-1-yl}methanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Quetiapine, open ring- | HCID 11338588 | — |
| Product | 2-(2-Acetamino-phenylsulfanyl)-phenyl-{4(2-(2-acetoxyethoxy)ethyl]piperazin-1-yl}methanone | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07863441B2 |
| Source dataset | uspto-grants-2011_01 |
| ORD ID | ord-0a4aed533096481791fefbef47eebc41 |
| Source note | uspto-grants-2011_01 |