HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloroethane → HCID 24744053, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | 4'-(Octyloxy)-[1,1'-biphenyl]-4-carboxylic acid | HCID 2802556 | — |
| Reactant | HCID 66755815 | HCID 66755815 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Dimethylformamide toluene | HCID 21735183 | — |
| Product | HCID 24744053 | HCID 24744053 | — |
Reaction Steps
1.06 mmol of 4′-(octyloxy)-4-biphenyl-carboxylic acid, 1.06 mmol of EDC and 1.06 mmol DIPEA are added to a mixture of 0.53 mmol of 5-(3-amino-phenyl)-1,1-dioxo-1,2,5-thiadiazolidin-3-one and 0.11 mmol of HOAt in 6 ml of a DMF/toluene-mixture. The mixture obtained is stirred at rt for 18 hours, diluted with EtOAc and toluene and a precipitate is obtained and filtered off. 4′-Octyloxy-biphenyl-4-carboxylic acid [3-(1,1,4-trioxo-1,2,5-thiadiazolidin-2-yl)phenyl]-amide in solid form is obtained. The filtrate obtained is washed with HCl (1M) and brine, the organic layer is dried and solvent is evaporated. Further 4′-octyloxy-biphenyl-4-carboxylic acid [3-(1,1,4-trioxo-1,2,5-thiadiazolidin-2-yl)-phenyl]-amide is obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08119617B2 |
| Source dataset | uspto-grants-2012_02 |
| ORD ID | ord-0b7cf361b4f045e1acc5e73accea5a85 |
| Source note | uspto-grants-2012_02 |