HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → 6-Carboxyfluorescein
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 6-Carboxyfluorescein | HCID 76806 | — |
| Reactant | N-Hydroxysuccinimide | HCID 80170 | — |
| Reactant | 5-Amino-2-ethylpentanoic acid | HCID 19880126 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 6-Carboxyfluorescein | HCID 76806 | — |
| Product | HCID 131715159 | HCID 131715159 | — |
Reaction Steps
An active ester of carboxyfluorescein was prepared by dissolving N-hydroxysuccinimide (5 mg), carboxyfluorescein (7.5 mg) and N,N'-dicyclohexylcarbodiimide (20 mg) in 0.5 ml of pyridine. The reaction was allowed to proceed for two hours at room temperature, after which time 2-ethyl-5-aminopentanoic acid (20 mg) was dissolved in the reaction mixture. The resulting mixture was allowed to react overnight in the dark at room temperature and the reaction product was purified twice employing silica gel thin-layer chromatography using a chloroform:methanol (3:1) mixture as developing solvent to yield a 2-ethyl-5-aminopentanoic acid-carboxyfluorescein conjugate of the formula: ##STR12##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05066426 |
| Source dataset | uspto-grants-1991_11 |
| ORD ID | ord-caec3513a1394141b0fc7bd0d898dbeb |
| Source note | uspto-grants-1991_11 |