HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → (2R)-2-({Formyl[(phenylmethyl)oxy]amino}methyl)hexanoyl fluoride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Cyanuric fluoride | HCID 12664 | — |
| Reactant | (2R)-2-({Formyl[(phenylmethyl)oxy]amino}methyl)hexanoic acid | HCID 11185069 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | (2R)-2-({Formyl[(phenylmethyl)oxy]amino}methyl)hexanoyl fluoride | HCID 86706342 | 100% |
Reaction Steps
To a solution of (2R)-2-({formyl[(phenylmethyl)oxy]amino}methyl)hexanoic acid (9) (1.7 g, 6.1 mmol) in DCM (20 mL) was added pyridine (0.53 g, 6.7 mmol), followed by 2,4,6-trifluoro-1,3,5-triazine (0.86 g, 6.4 mmol) dropwise. The reaction mixture was stirred for 4 h and TLC indicated completion of the reaction. The reaction mixture was washed with 10% aqueous citric acid and brine, dried over Na2SO4, and concentrated to provide the title compound (1.7 g, 100%) as red oil. 1H NMR (300 MHz, DMSO) δ ppm 0.86 (t, J=6.7 Hz, 3H), 1.16-1.38 (m, 4H), 1.57 (m, 2H), 3.03 (m, 1H), 3.87 (m, 2H), 4.91 (s, 2H), 7.41 (m, 5H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08901119B2 |
| Source dataset | uspto-grants-2014_12 |
| ORD ID | ord-13737076165644e5a45aac3e696ee427 |
| Source note | uspto-grants-2014_12 |