HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → ((R)-1-dimethylcarbamoyl-3-methyl-butyl)-carbamic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Dimethylamine, hydrochloride | HCID 10473 | — |
| Reactant | PyBOP | HCID 2724699 | — |
| Reactant | BOC-D-LEU-OH H2O | HCID 2724763 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | ((R)-1-dimethylcarbamoyl-3-methyl-butyl)-carbamic acid tert-butyl ester | HCID 28165661 | 58% |
Reaction Steps
To a solution of Boc-D-leucine monohydrate (2.0 g, 8.0 mmol), triethylamine (5.6 mL, 40.1 mmol), and dimethylamine hydrochloride (1.31 g, 16.0 mmol) in DMF (15 mL) at room temperature was added PyBOP (4.59 g, 8.82 mmol). The reaction mixture was stirred overnight then diluted with EtOAc (50 mL) and washed with water (4×50 mL). The combined organic extracts were dried (Na2SO4) and evaporated under vacuum. The crude residue was purified by SiO2 chromatography (80 g, hexanes/EtOAc, 1:1) to give 1.19 g (58%) of ((R)-1-dimethylcarbamoyl-3-methyl-butyl)-carbamic acid tert-butyl ester as a colorless viscous oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08481541B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-948d16f949124e3abb92073d9e0fda0f |
| Source note | uspto-grants-2013_07 |