HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → ethyl 12-aMinododecanoate hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 12-Aminododecanoic Acid | HCID 69661 | — |
| Reactant | 4-Chloro-3-nitroquinoline | HCID 11275808 | — |
| Reactant | ethyl 12-aMinododecanoate hydrochloride | HCID 57447050 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | ethyl 12-aMinododecanoate hydrochloride | HCID 57447050 | — |
| Product | HCID 57447051 | HCID 57447051 | — |
Reaction Steps
Ethyl 12-aminododecanoate hydrochloride was prepared from 12-aminododecanoic acid, thionyl chloride, and ethanol by the general method of C. Temple, Jr., R. D. Elliott, and J. A. Montgomery, J. Med. Chem., 1988, 31, 697-700. The general method described in Step 1 of Example 15 was used to react 4-chloro-3-nitroquinoline (15.5 g, 74.4 mmol), ethyl 12-aminododecanoate hydrochloride (25.0 g, 89.3 mmol), and triethylamine (18.8 g, 186 mmol) in dichloromethane for 15 hours to provide ethyl 12-(3-nitroquinolin-4-ylamino)dodecanoate (30.0 g) as a yellow solid that was used directly in the next step without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09328110B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-47ab3dfc286d4149a7b83578fdaa7a7a |
| Source note | uspto-grants-2016_05 |