HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → 5-(3-(2-(7-Chloroquinolin-2-YL)ethyl)phenyl)-8-dimethylcarbamyl-4,6-dithiaoctanoic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | 2-Chloro-1-methylpyridinium iodide | HCID 167069 | — |
| Reactant | HCID 10413257 | HCID 10413257 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | 5-(3-(2-(7-Chloroquinolin-2-YL)ethyl)phenyl)-8-dimethylcarbamyl-4,6-dithiaoctanoic acid | HCID 19930521 | — |
Reaction Steps
To a suspension of diacid (Example 25) (0.3 g) in dichloromethane (20 mL), acetonitrile (5 mL) and triethylamine (200 μL) was added 2-chloro-1-methylpyridinium iodide (180 mg). The mixture was stirred 30 min, cooled to 0° and 0.32 mL of a 2M solution of dimethylamine in toluene was added. The reaction was stirred 2 hours at room temperature. The reaction mixture was poured onto NH4OAc buffer and acetic acid (5 mL) was added. The mixture was extracted with ethyl acetate, which was dried over sodium sulfate and evaporated. Purification of the residue by flash chromatography starting with 15% and finishing with 30% of THF in toluene containing 1% of acetic acid afforded the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05428171 |
| Source dataset | uspto-grants-1995_06 |
| ORD ID | ord-6a7ee6954ddc497abbbbcc193478656f |
| Source note | uspto-grants-1995_06 |