HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → {(R)-1-[Allyl-(2,4-dimethoxy-benzyl)-carbamoyl]-but-3-enyl}-carbamic acid tert-butyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 4722371 | HCID 4722371 | — |
| Reactant | O-(7-Azabenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium Tetrafluoroborate | HCID 11099301 | — |
| Reactant | Boc-L-allylglycine . DCHA | HCID 53395397 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | {(R)-1-[Allyl-(2,4-dimethoxy-benzyl)-carbamoyl]-but-3-enyl}-carbamic acid tert-butyl ester | HCID 57589913 | — |
Reaction Steps
(R)-N-Boc-allylglycine (2.3 g, 9.9 mmol) was dissolved in dimethylformamide (20 ml) and activated with the coupling reagent TATU (3.5 g, 10.9 mmol) and Hünig's base (3.8 ml, 21.9 mmol) for 2 min. Allyl-(2,4-dimethoxy-benzyl)-amine (2.1 g, 9.9 mmol) dissolved in dimethylformamide (20 ml) was added to the chilled (ice-water bath) reaction mixture and the stirring was continued overnight. The solvent was evaporated and the residue was dissolved in ethyl acetate, washed with saturated NaHCO3 solution, 1 M KHSO4 solution, brine, dried (MgSO4.2H2O), filtered and concentrated under reduce pressure and purified over silica gel (ethyl acetate/n-heptane 1:4): colorless gum 2.6 g (62%);
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07501406B2 |
| Source dataset | uspto-grants-2009_03 |
| ORD ID | ord-8c66eddc371c43c7a53c3ee05b304da1 |
| Source note | uspto-grants-2009_03 |