HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 10447619, compound → 2-(1H-Imidazol-1-yl)-1-{2-[(2-methoxyphenoxy)methyl]-1,3-thiazolidin-3-yl}ethan-1-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 10447619 | HCID 10447619 | — |
| Reactant | HCID 178507081 | HCID 178507081 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 2-(1H-Imidazol-1-yl)-1-{2-[(2-methoxyphenoxy)methyl]-1,3-thiazolidin-3-yl}ethan-1-one | HCID 3025456 | 79.6% |
Reaction Steps
Imidazolyl sodium (3.58 g) is added to a stirred solution of 3-chloroacetyl-2-(o-methoxyphenoxy)methylthiazolidine (5.8 g) in DMSO (35 ml). After 1 hour the mixture is poured in ice and water (200 ml) and the separated oil is extracted with EtOAc (3×30). The organic phases are collected, washed with water, dried on Na2SO4. After evaporation, the crude residue is purified by filtration on a short column of SiO2 using EtOAc and EtOAc/MeOH 85:15 as the eluent to give 3-(imidazol-1-yl)acetyl-2-(o-methoxyphenoxy)methyl-thiazolidine (5.1 g) as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04798898 |
| Source dataset | uspto-grants-1989_01 |
| ORD ID | ord-e45f96d681134d22b0dac77ac75044d0 |
| Source note | uspto-grants-1989_01 |