HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethylmorpholine → HCID 58031792, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethylmorpholine | HCID 7525 | — |
| Reactant | Dimethyl malonate | HCID 7943 | — |
| Reactant | Malonate Ion | HCID 9084 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | 2-(3-TERT-BUTYLPHENOXY)PROPANOIC ACID | HCID 16770162 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 58031792 | HCID 58031792 | 74% |
Reaction Steps
To a solution of 250 mg (0.91 mmol) of dimethyl malonate, malonate, 314 mg (2.72 mmol) of N-ethylmorpholine, 153 mg (1.0 mmol) of HOBt hydrate and 155 mg (1.0 mmol) of EDAC in 7 ml of DMF was added a solution of 202 mg (0.91 mmol) of 2-(3-tert-butylphenoxy)propionic acid in 3 ml of DMF. After 18 h at room temperature, the reaction mixture was concentrated completely and separated by means of preparative HPLC (Merck Hibar Purospher Star RP-18e 10 μm 25×250 mm; A: H2O+0.05% TFA; B: ACN+0.05% TFA; flow rate: 50 ml/min; in 15 minutes 10% B→90% B). The product fractions were freeze-dried to give 323 mg (74%) of dimethyl 2-(1-{4-[2-(3-tert-butylphenoxy)propionylamino]phenyl}but-2-ynyl)malonate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08648038B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-e2a33a9e7c614756bacfb986dfeaf445 |
| Source note | uspto-grants-2014_02 |