HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → HCID 68157210, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | Tert-butoxycarbonylalanine | HCID 85082 | — |
| Reactant | HOAt | HCID 181649 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | HCID 19043380 | HCID 19043380 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 68157210 | HCID 68157210 | — |
Reaction Steps
A mixture of 4-fluoro-N1-phenylbenzene-1,2-diamine (866 mg, 4.3 mmol), (S)-2-tertbutoxycarbonylaminopropionic acid (890 mg, 4.7 mmol), HOAt (640 mg, 4.7 mmol), 4-methylmorpholine (1.0 mL, 9.5 mmol) and N-(3-dimethylaminopropyl)-N′-ethylcarbodiimide hydrochloride (900 mg, 4.7 mmol) in DCM (20 mL) was stirred at RT for 2 h. The reaction mixture was partitioned between DCM and a saturated aqueous solution of NaHCO3. The organic fraction was washed with brine, dried (MgSO4) and concentrated in vacuo to afford the title compound as a yellow-orange solid (quantitative). The crude product was used in the following step without further purification. LCMS (Method B): RT 3.83 min [M+H]+ 374.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08653089B2 |
| Source dataset | uspto-grants-2014_02 |
| ORD ID | ord-1bca935187b54c3c8d07a781e0b76e52 |
| Source note | uspto-grants-2014_02 |