HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Methylmorpholine → HCID 67548010, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Methylmorpholine | HCID 7972 | — |
| Reactant | HCID 11666699 | HCID 11666699 | — |
| Reactant | HCID 58515553 | HCID 58515553 | — |
| Reactant | HCID 86600267 | HCID 86600267 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67548010 | HCID 67548010 | — |
Reaction Steps
To a stirred solution of 2(R)-amino-3-cyclopropylmethylsulfanylpropan-1-ol (80.5 mg, 0.5 mmol) in anhydrous THF (3 mL) were added activated 4 Å molecular sieves (250 mg) and N-methylmorpholine (51 mg, 0.5 mmol). After stirring for 10 min, trifluoromethanesulfonic acid 2,2,2-trifluoro-1-phenylethyl ester (190.5 mg, 0.5 mmol) was added and the reaction was stirred at room temperature for 2 days. The reaction mixture was filtered and the filtrate was concentrated. The residue was purified by flash column chromatography to afford the desired mixture of diastereomers of 2(R)-3-cyclopropylmethyl-sulfanyl-2-(2,2,2-trifluoro-1(RS)-phenylethylamino)propan-1-ol. LC-MS: 318.3(M-1), 320.8(M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07737300B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-0739ed8068804de2b7dc47c0fc3d1cd5 |
| Source note | uspto-grants-2010_06 |