Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isoamyl Nitrite | HCID 8053 | — |
| Reactant | HCID 131713890 | HCID 131713890 | — |
| Reactant | HCID 131713892 | HCID 131713892 | — |
| Reactant | HCID 178427532 | HCID 178427532 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| Product | HCID 178427530 | HCID 178427530 | — |
Reaction Steps
0.39 Gram of Z-Leu-Gly-NHNH2 was dissolved in 5 ml of dimethylformamide and 0.58 ml of 6N HCl/dioxane, then a reaction similar to that described in Reference example 1 was carried out by using 10 ml of a dimethylformamide solution containing 0.15 ml of isoamyl nitrite, 0.49 ml of triethylamine and 1.00 g of H-Phe-Leu-Gln-Arg(Tos)-Ser-Ser-OH, further an equivalent amount of Z-Leu-Gly-N3 was added to the reaction mixture and reacted at 4° C. for 20 hours. The reaction mixture was extracted with butanol, the extract was washed with 2%-acetic acid, then butanol and acetic acid were removed by sistillation, the residue was crystallized from ether. The crystals were collected by filtration and washed with a hot methanol to obtain 0.65 g of Z-Leu-Gly-Phe-Leu-Gln-Arg(Tos)-Ser-Ser-OH.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US04474754 |
|---|
| Source dataset | uspto-grants-1984_10 |
|---|
| ORD ID | ord-0c13fa23f5544eac96413fd774babaa3 |
|---|
| Source note | uspto-grants-1984_10 |
|---|