HuagongsheHuagongshe Chemistry Print Report · For research reference only
Z-Gly-Phe-NHNH-COCH3 → H-Gly-Phe-NHNH-COCH3
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Z-Gly-Phe-NHNH-COCH3 | HCID 12919697 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | H-Gly-Phe-NHNH-COCH3 | HCID 131712285 | 26.4% |
Reaction Steps
Z-Gly-Phe-NHNH-COCH3 (5 g) is hydrogenated over a Pd-black as a catalyst in MeOH (100 ml). The catalyst is filtered and the filtrate is evaporated to give 3.5 g of H-Gly-Phe-NHNH-COCH3 as crystals, H-Gly-Phe-NHNH-COCH3 (0.89 g) and Z-(D)-Nva-ONB, which is prepared from Z-(D)-Nva-OH (0.80 g) and HONB (0.63 g) by the DCC method, are dissolved in DMF (10 ml). The mixture is stirred for 10 hr. at room temperature and evaporated. The residue is treated with diethylether to give a powder which is crystallized from acetonitrile; yield 1.3 g. m.p. 235°-237° C., [α]D23 +3.4° (c=0.45, DMF), Rf1 =0.44.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04277394 |
| Source dataset | uspto-grants-1981_07 |
| ORD ID | ord-f8d78ef0f1ea43b0824acf41475499e7 |
| Source note | uspto-grants-1981_07 |