HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → Z-Phe-gly-NH2
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Glycinamide hydrochloride | HCID 2723639 | — |
| Reactant | Z-Phe-OBzl | HCID 7016068 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | Z-Phe-gly-NH2 | HCID 7020269 | 100.2% |
Reaction Steps
To a solution of Z-L-Phe-OBn (25, 19.2 mg, 0.05 mmol) in DMF (0.25 mL) and water (0.144 mL), glycinamide hydrochloride (31, 17 mg, 0.15 mmol) and Et3N (0.15 mmol, 0.0625 mL) were added, followed by the addition of S166C—S-inden-oxaz(S,R) (ME-n, 0.106 mL, 0.5 mg of active enzyme in 10 mM MES buffer (pH 5.8) including 1 mM CaCl2). The reaction was stirred for one hour at room temperature. The mixture was diluted with AcOEt and washed with 1 M KHSO4 (1 mL×1) and brine (1 mL×1), and the organic layer was dried over MgSO4. After evaporation, the residue was purified by preparative TLC (CH2Cl2/MeOH=90/10) to afford Z-L-Phe-Gly-NH2 (33, 17.8 mg, quantitative).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06395532B1 |
| Source dataset | uspto-grants-2002_05 |
| ORD ID | ord-19a5def99f8242c8a74e5590bbd1bb43 |
| Source note | uspto-grants-2002_05 |