HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloroethane → HCID 54138481, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | 4-(4-Nitrophenyl)butyric acid | HCID 79711 | — |
| Reactant | HCID 67553617 | HCID 67553617 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 54138481 | HCID 54138481 | — |
Reaction Steps
4-(4-Nitrophenyl)butyric acid (73 mg, 350 μmol), dissolved in DMF (5 ml) was treated with HOBT (60 mg, 350 μmol), EDC (76 mg, 350 μmol) and N-[2(S)-amino-3-methylpentyl)-N-(1-naphthylmethyl)-glycyl-methionine methyl ester hydrochloride (160 mg, 300 μmol). The pH was adjusted to ~7.5 with Et3N (170 μl, 385 μmol) and the mixture was stirred at ambient temperature for 16 h. The mixture was concentrated and the residue was partitioned between EtOAc (100 ml) and H2O (100 ml). The organic layer was washed with H2O (2×50 ml), dried (MgSO4), filtered and concentrated to give a crude product which was purified by chromatography (silica gel, eluting with 1:1 to 1:2 hexane: EtOAc) to give the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05523456 |
| Source dataset | uspto-grants-1996_06 |
| ORD ID | ord-3158d2122d1846509c90ea07f60e7b03 |
| Source note | uspto-grants-1996_06 |