HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dicyclohexylcarbodiimide → Boc-Asp(OBzl)-NHMe
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N-tert-Butoxycarbonyl-L-aspartic acid beta-benzyl ester | HCID 1581888 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Reactant | HCID 178418300 | HCID 178418300 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Boc-Asp(OBzl)-NHMe | HCID 59516205 | 58.6% |
Reaction Steps
Boc-Asp(OBzl) (6.4 g) was dissolved in tetrahydrofuran (30 ml), added with dicyclohexylcarbodiimide (4.1 g), hydroxybenzotriazole (3.0 g), methylamine hydrochloride (2.0 g) and diisopropylethylamine (3.9 g) under ice cooling and stirred for 10 hours. Insolubles were removed from the mixture by filtration and the filtrate was concentrated under reduced pressure. The residue was dissolved in ethyl acetate and the organic layer was washed with 10% aqueous solution of citric acid and saturated aqueous solution of sodium hydrogen carbonate and dried over anhydrous sodium sulfate. Then the ethyl acetate was evaporated under reduced pressure. The residue was recrystallized from ethyl acetate/hexane to give Boc-Asp(OBzl)-NHMe (3.9 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05763408 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-df6ae7d590dc4e59bae0eef0e6407b33 |
| Source note | uspto-grants-1998_06 |