HuagongsheHuagongshe Chemistry Print Report · For research reference only
Aminoisobutyric acid → N-[4-(hexadecylamino)benzoyl]-2-methylalanine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Aminoisobutyric acid | HCID 6119 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | N-[N-trifluoroacetyl-4-(hexadecylamino)benzoyloxy]succinimide | HCID 20437360 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Water | HCID 962 | — |
| Product | N-[4-(hexadecylamino)benzoyl]-2-methylalanine | HCID 20437359 | — |
Reaction Steps
To a stirred solution of 103 mg. of 2-aminoisobutyric acid and 4.5 ml. of triethylamine in 1.5 ml. of water is added a solution of 550 mg. of N-[N-trifluoroacetyl-4-(hexadecylamino)benzoyloxy]succinimide in 4.5 ml. of ethanol. The mixture is stirred for 23 hours at room temperature, treated with 2 ml. of 2 N sodium hydroxide solution, and then acidified. The mixture is diluted with water and then filtered. Recrystallization from ether-hexane affords the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04242273 |
| Source dataset | uspto-grants-1980_12 |
| ORD ID | ord-fa57c209328748a5a33266d6a7a21c9a |
| Source note | uspto-grants-1980_12 |