HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → N-(N'-Acetylglycyl) sphingosine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Acetylglycine | HCID 10972 | — |
| Reactant | Sphingosine | HCID 5280335 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | N-(N'-Acetylglycyl) sphingosine | HCID 86749485 | — |
Reaction Steps
5.0 gr of sphingosine (16.70 mM), prepared according to Example 4, 2.1 gr of N-acetylglycine (18.37 mM) and 3.8 gr of dicyclohexylcarbodiimide (18.40 mM) are left to react in 150 cc of chloroform, under warm conditions overnight. The reaction mixture is placed in a freezer to precipitate. The urea is filtered, and the chloroform solution is washed with H2O. The raw material is purified by chromatography using a mixture of CH2Cl2 /ethyl acetate/CH3OH, 70:30:10 v/v/v.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05792858 |
| Source dataset | uspto-grants-1998_08 |
| ORD ID | ord-a8a5b36237b34e708ce4fddf06792b27 |
| Source note | uspto-grants-1998_08 |