HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 178475065, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 178446354 | HCID 178446354 | — |
| Reactant | HCID 178446355 | HCID 178446355 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178475065 | HCID 178475065 | — |
Reaction Steps
To the deprotected Lys-resin sample was added Fmoc-Phe (8.8 mg, 33.2 μmol) in DCM/DMF and 1,3-diisopropylcarbodiimide (DIC) (3 μL, 20 μmol). The coupling reaction was continued for 2 h and ninhydrin tests gave negative amino group readings. The Fmoc-Phe-Lys(ivDde) on resin was then treated with photogenerated piperidine as described above. Upon completion of the reaction, the resin was washed with DCM/DMF. Capping of the NH2-Phe-Lys(ivDde)-resin was carried out for 1 h with acetic anhydride (470 μL, 5 mmol) and TEA (700 μL, 5 μmmol) in 1.5 mL DMF to give Ac-Phe-Lys(ivDde)-resin.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06965040B1 |
| Source dataset | uspto-grants-2005_11 |
| ORD ID | ord-9667d6b1f38f48aaa3e1e73373a421e0 |
| Source note | uspto-grants-2005_11 |