HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,2-Dichloroethane → Fmoc-Indanylglycine Val-OAllyl
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,2-Dichloroethane | HCID 11 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Fmoc indanylglycine | HCID 68451954 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Fmoc-Indanylglycine Val-OAllyl | HCID 131731716 | — |
Reaction Steps
Fmoc Indanylglycine (0.54 g, 1.315 mmol) was solvated in CH2Cl2 (5 mL) and DMF (1.8 mL) followed with the addition of L-Val allylester (0.437 g, 1 eq), 4-methylmorpholine (0.15 ml, 1.04 eq) and 4 min latter DMAP (14.5 mg, 0.09 eq) then EDC (0.265 g, 1.05 eq). The mixture was stirred for 1 hour 45 min. Then it was extracted using EtOAc/brine. The organic layer was dried over MgSO4, filtered off and concentrated to dryness.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09045524B2 |
| Source dataset | uspto-grants-2015_06 |
| ORD ID | ord-2dcd0d3f55194d44a444e81d83f775c3 |
| Source note | uspto-grants-2015_06 |